Manufacturing & Production

Amgen

Manufacturing Systems Engineer: Automation

**Join Amgens Mission of Serving Patients**

At Amgen, if you feel like youre part of something bigger, its because you are. Our shared missionto serve patients living with serious illnessesdrives all that we do.

Since 1980, weve helped pioneer the world of biotech in our fight against the worlds toughest diseases. With our focus on four therapeutic areas Oncology, Inflammation, General Medicine, and Rare Disease we reach millions of patients each year. As a member of the Amgen team, youll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.

Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lie within them, youll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

Be part of Amgen's newest and most advanced drug substance manufacturing plant. When completed, the Amgen FleX Batch facility will combine the latest in disposable technologies with traditional stainless-steel equipment to allow for maximum flexibility in operations. The FleX Batch facility will not only feature the best in-class drug substance manufacturing technologies with embedded industry 4.0 capabilities, but it will also integrate sustainability innovations to reduce carbon and waste, as part of Amgen's plan to be a carbon-neutral company by 2027.

**Manufacturing Systems Engineer: Automation**

**What you will do**

Lets do this. Lets change the world. As a Manufacturing Systems Engineer, you will work with a group of automation engineers who are responsible for building and maintaining various automation systems and platforms that support the GMP DrugSubstancePlant Operations.

In this vital roleas a member of the Facilities & Engineering (F&E) Automation teamyou will work hand in hand with the capital project team to deliver robust process automation systems to operate the new plant.

Responsibilities:

- Develop and maintain the process control system on Emerson DeltaV distributed control system (DCS).

- Collaborate with key stakeholders and end-users to understand and synthesize key process requirements, and to develop solutions using Amgen standard automation platform for process automation systems.

- Provide clear documentation for delivered solutions and processes.

- Support QA partners in performing computerized systems validation in a GxP environment.

- Perform Data Integrity Assessments (DIA) in accordance with the current Amgen and industry standards.

- Support process automation systems to ensure design aligns with Amgen specifications, incorporates the latest technology, and meets safety requirements.

- Support vendor FAT to ensure that control strategy and software code meet Amgen requirements.

- Develop and maintain engineering and maintenance documentation, and associated procedures for delivered solutions and processes.

- Support commissioning and qualification efforts including Automation Installation Verification/Automation Check Out (IV/ACO) in a fast-paced environment.

- **Site Operations**

- Own and drive to completion Change Controls, CAPAs, and Deviations.

- Support technical root cause analysis, incident investigations, and troubleshooting.

- Support functional area projects focused on improving process equipment, utilities, and facilities as well as large capital projects to integrate new drug substance manufacturing technologies into the facility.

- Drive continuous improvement for process automation systems to improve operational workflows, safety, reliability, efficiency, and sustainability.

- Support day-to-day operations including rotational on-call support.

- Prepare/review Standard Operating Procedures (SOP) and cGMP documents.

- Be constantly curious and feed your passion and interests in groundbreaking technology. Use your given time to look for new and innovative ways to do business differently, better, and more cost effectively.

**What we expect from you**

We are all different, yet we all use our unique contributions to serve patients. The automation professional we seek is an engineer with these qualifications.

**Basic Qualifications**

- High School Diploma / GED and 8 years of Engineering experience OR

- Associates Degree and 6 years of Engineering experience OR

- Bachelors Degree and 2 years of Engineering experience OR

- Masters Degree

**Preferred Qualifications**

- Degree in Electrical Engineering, Computer Science, Chemical Engineering, Biotech Engineering, or related field.

- Direct knowledge of Automation System design, experience in process control engineering and troubleshooting with GMP biopharmaceutical production facility equipment/systems automation such as media, harvest, bioreactors, solution prep, single use mixing vessels, chromatography, TFFL/TFFX, viral filtration, viral inactivation, UF/DF, depth filtration, drug substance fill, CIP/SIP, clean utilities, and integrating various OEM automation software.

- Experience in programming, installation, and lifecycle management of automation and field instrumentation technologies.

- Experience in programming, design, installation and lifecycle management of manufacturing process controls, and automation and field instrumentation technologies.

- Experience with Emerson DeltaV DCS system and ability to perform advanced troubleshooting, and system integration using OPC, Foundation Fieldbus, and Profibus technologies.

- Ability to interpret and apply GAMPs and GMPs, and familiarity with documentation in a highly regulated environment with requirements such as 21 CFR Part 11, ASTM 2500, S88 and S95.

- Self-directed team player able to work cross-functionally.

- Strong technical writing and communication skills.

**What you can expect from us**

As we work to develop treatments that take care of others, we also work to care for our teammates professional and personal growth and well-being. From our competitive benefits to our collaborative culture, well support your journey every step of the way.

In addition to the base salary, Amgen offers a Total Rewards Plan based on eligibility that may include:

- A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts

- A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan

- Stock-based long-term incentives

- Award-winning time-off plans and bi-annual company-wide shutdowns

- Flexible work models, including remote work arrangements, where possible

**Apply now for a career that defies imagination**

In our quest to serve patients above all else, Amgen is the first to imagine and the last to doubt. Join us.

careers.amgen.com

\#AmgenNorthCarolina

North Carolina

Undergrad Co-op MCS Manufacturing Associate

**Join Amgens Mission of Serving Patients**

At Amgen, if you feel like youre part of something bigger, its because you are. Our shared missionto serve patients living with serious illnessesdrives all that we do.

Since 1980, weve helped pioneer the world of biotech in our fight against the worlds toughest diseases. With our focus on four therapeutic areas Oncology, Inflammation, General Medicine, and Rare Disease we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, youll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.

Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, youll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

**Undergrad Co-op MCS Manufacturing Associate**

**What You Will Do**

Lets do this. Lets change the world. During this undergraduate cooperative, you will work as a Manufacturing Associate in the Durg Substance (DS)/Drug Product (DP) Technical Operations within the Manufacturing Clinical Supply Organization. This team is responsible for supplying Amgens portfolio of clinical trials currently underway, globally. The co-op will be responsible for an improvement project and exposed to a dynamic clinical manufacturing environment. Project may include:

- Working closely across multiple subject areas, including Process Development, Facilities & Engineering, and Manufacturing to execute a diverse portfolio of projects
- Execute problem solving, root cause analysis and data visualization
- Leveraging standard Continuous Improvement principles to devise new solutions
- Identifying opportunities to optimize workflows and protocols to increase throughput in the manufacturing process
- Evaluate procedural improvement opportunities
- Conduct production floor testing, including coordination amongst multiple teams and disciplines

**Program Eligibility Requirements**

- Expected completion of one year of study from an accredited college or university prior to the internship commencing
- Expected continued enrollment in an accredited college or university following the internship program
- Student must be located in the United States for the duration of the internship program
- Must be available to work a part-time schedule

**What We Expect of You**

We are all different, yet we all use our unique contributions to serve patients. The creative and analytical individual we seek is a team player with these qualifications:

**Basic Qualifications:**

Amgen requires that all individuals applying for an undergrad internship or a co-op assignment at Amgen must meet the following criteria:

- 18 years or older
- Currently enrolled in a full-time Bachelors Degree program from an accredited college or university with a 3.0 minimum GPA or equivalent

**Preferred Qualifications**

- Degree concentration(s) in Engineering or Life Sciences
- Previous experience in biology lab
- Prior work or volunteering experience
- Ability to work effectively in cross functional teams
- Familiarity with Microsoft Office and collaboration tools (e.g., PowerPoint, Microsoft Teams, Smartsheet, Tableau)
- Good communication skills and writing skills
- Analytical thinking
- Proactiveness
- Project Management Experience

**What You Can Expect of Us**

As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, well support your journey every step of the way.

The base pay range for this opportunity in the U.S. is $28.87 per hour.

- Build a network of colleagues that will endure and grow throughout your time with us and beyond.
- Bring your authentic self to the table and become the professional youre inspired to be through accepting a culture that values the diversity of thought and experience and will flex to your strengths and possibilities.
- Participate in executive and social networking events, as well as community volunteer projects.

**Apply now and make a lasting impact with the Amgen team.**

**careers.amgen.com** Please search for Keyword R-256774

In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.

**Application deadline**

Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.

**Sponsorship**

Candidates must be authorized to work in the U.S. for the duration of this program. Sponsorship for future FTE roles is not guaranteed.

As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.

Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

California

Senior Manufacturing Systems Engineer (DeltaV/PLC)

Join Amgens Mission of Serving Patients

At Amgen, if you feel like youre part of something bigger, its because you are. Our shared missionto serve patients living with serious illnessesdrives all that we do.

Since 1980, weve helped pioneer the world of biotech in our fight against the worlds toughest diseases. With our focus on four therapeutic areas Oncology, Inflammation, General Medicine, and Rare Disease we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity-related conditions. As a member of the Amgen team, youll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.

Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, youll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

**Senior Manufacturing Systems Engineer (DeltaV/PLC)**

**What you will do**

Lets do this. Lets change the world. In this role as a member of the Amgen Manufacturing & Clinical Supplies Facilities & Engineering (MCS-F&E) Automation team you will support Clinical and Commercial Drug Substance plant operations. This includes complex and challenging system automation initiatives that require understanding of various automation platforms, integration between multiple platforms, analytical problem-solving techniques, critical thinking, project management, lifecycle management and Operational Excellence.

**Responsibilities include:**

- Develop and maintain process control automation solutions applying DeltaV Distributed Control System (DCS), Rockwell Programmable Logic Controllers (PLC), Human Machine Interfaces (HMI), Supervisory Control and Data Acquisition systems (SCADA
- Lead/support technical root cause analysis, incident investigations, and trouble shooting on process control issues related to plant operations.
- Own change control records, CAPA records and deviations as it relates to Automation systems.
- Support functional area projects focused on improving process equipment, cleaning systems and utilities to ensure reliability of drug substance manufacturing facility.
- Lead and support new technology introductions by performing automation engineering assessments, implementing automation system configuration changes, and supporting engineering and process qualification runs as applicable.
- Provide Continuous Improvement initiatives including Safety, Reliability, Efficiency and Environmental sustainability improvements to meet Amgens Ambitious goals.
- Maintain Data Integrity Assessments with the current Amgen and Industry standards.
- Support Review by Exception (RbE) functionality that includes product Batch records, cleaning, and sterilization systems, Audit trail and version control systems.
- Collaborate with Amgen Drug Substance Plant network to enhance the automation design for Drug Substance Plant Operations
- Be knowledgeable about compliance and regulatory aspects for operation and maintenance, equipment validation, and support regulatory inspections and audits.

**Day-to-day Operational Support including:**

- Direct Manufacturing Support required for Critical Operations
- 24 x 7 On Call on a rotational basis.
- Troubleshooting support to Manufacturing operations, cleaning systems, plant utilities and Building management system
- Automation System Administration
- Automation System Operating Systems (OS) security patching and HotFix assessments and rollout
- Daily manufacturing and engineering work center team meetings
- Preventative and corrective maintenance
- Automation System spare parts management

**What we expect of you**

We are all different, yet we all use our unique contributions to serve patients. The Automation professional we seek has these qualifications:

**Basic Qualifications:**

- Doctorate degree OR
- Masters degree and 3 years of Manufacturing Automation Engineering experience OR
- Bachelors degree and 5 years of Manufacturing Automation Engineering experience OR
- Associate degree and 8 years of Manufacturing Automation Engineering experience OR
- High school diploma / GED and 10 years of Manufacturing Automation Engineering experience

**Preferred Qualifications:**

- Extensive understanding and background in programming, design, installation, and lifecycle management of manufacturing process controls, automation, and field instrumentation technologies.
- Demonstrated hands-on experience in developing process control strategies in Clinical/Commercial Drug Substance Plant Operations.
- Familiarity with Upstream and Downstream unit operations.
- Direct knowledge of Automation design, experience in process control engineering and trouble shooting with GMP biopharmaceutical production facility equipment/systems such as media, harvest, bioreactors, chromatography, filtration and ultrafiltration/diafiltration, and integrating various OEM automation software.
- Demonstrated experience with continuous improvements resulting in enhanced safety, system reliability, and productivity (e.g., cycle times; reduced plant utilities usage) related to Drug Substance Plant Operations.
- Experience in Capital Project Lifecycle Management: Conceptual Design, Scope, and cost estimate development, case development, detailed design, engineering and validation documentation and project execution are a plus.
- The ideal individual must be a self-directed standout colleague ready to mentor. engineering staff and embrace a team-based culture that relies on collaboration for effective decision-making.
- Strong leadership, technical writing, and communication/presentation skills.
- Ability to perform independently, self-motivated, organized, able to multi-task in project environments, and skilled in communication, facilitation, and collaboration.

**5+ years combined experience with the following:**

- Emerson Delta-V DCS system
- Rockwell Automation SCADA and PLC Platform.
- Electronic Batch Reporting Systems Design and implementation experience.
- Process Control Network design including network segregation.
- Process Control Systems: Virtual Infrastructure design and implementation and ability to perform advanced trouble shooting activities in coordination with Amgen IS.
- System Integration using OPC, Profibus, Serial VIM, Ethernet and DeviceNet technologies.
- Compliance and regulatory requirements such as 21 CFR Part 11, S88, S95 and GAMP.

**What you can expect from us**

As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, well support your journey every step of the way.

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.

In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:

- A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
- A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
- Stock-based long-term incentives
- Award-winning time-off plans
- Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.

Apply now and make a lasting impact with the Amgen team.

**careers.amgen.com**

In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.

Application deadline

Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.

Sponsorship

Sponsorship for this role is not guaranteed.

As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.

Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

Associate Manufacturing - Nights

**Join Amgens Mission of Serving Patients**

At Amgen, if you feel like youre part of something bigger, its because you are. Our shared missionto serve patients living with serious illnessesdrives all that we do.

Since 1980, weve helped pioneer the world of biotech in our fight against the worlds toughest diseases. With our focus on four therapeutic areas Oncology, Inflammation, General Medicine, and Rare Disease we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, youll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.

Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, youll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

**Associate manufacturing - Nights**

**What you will do**

Lets do this. Lets change the world. In this vital role you will perform operations in the Manufacturing area. Lets do this. Lets change the world.

Responsibilities Include:

- Operations will be performed according to Standard Operating Procedures (SOP's)
- Associate will perform and monitor critical processes, complete routine validation protocols and regularly draft and revise documents such as Manufacturing Procedures, SOP's and technical reports.
- Associate will also perform basic troubleshooting and assist in the review of documentation for assigned functions.
- May participate on cross-functional teams and represent the manufacturing teams.
- Associate may also have the responsibility of owning deviations/CAPA's.
- In addition, Associate may identify, recommend and implement improvements related to routine functions. In this vital role you will perform operations in the Manufacturing area. Operations will be performed according to Standard Operating Procedures (SOPs).

In this role, you will be expected to work a 12-hour shift (7PM-7AM) on a rotating schedule. This includes extra benefits such as**receiving an added 15% shift differential, and also getting premium pay for any Sundays worked.** The schedule during the initial on-boarding phase for this role (2-6 weeks) will be administrative (Monday through Friday, approximately 8am to 5pm)..

**What we expect of you**

We are all different, yet we all use our unique contributions to serve patients. The dedicated professional we seek is a great teammate with these qualifications.

**Basic Qualifications**:

- High school/GED + 2 years of manufacturing or operations work experience OR
- Associates + 6 months of manufacturing or operations work experience OR
- Bachelors Degree in a related field

**Preferred Qualifications**:

- Bachelors degree in Science or Engineering
- Knowledge of large-scale biotechnology operations such as purification, cell culture, aseptic processing, etc
- Knowledge of Single-use-Systems
- CFR and Regulatory knowledge
- Mechanical ability/expertise
- Basic statistical mathematical skills
- Ability to interpret and apply GMP knowledge
- Understanding of analytical methods for manufacturing area
- Demonstrated technical writing capability
- Able to demonstrate project management skills and presentation skills
- Ability to understand, apply and evaluate basic chemistry, biology and physical principles
- Basic troubleshooting skills on production equipment
- Experience with Delta V
- Experience with lab equipment/testing

**What you can expect of us**

As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, well support your journey every step of the way.

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.

In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:

- A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
- A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
- Stock-based long-term incentives
- Award-winning time-off plans
- Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.

**Apply now and make a lasting impact with the Amgen team.**

**careers.amgen.com**

In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.

**Application deadline**

Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.

**Sponsorship**

Sponsorship for this role is not guaranteed.

As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.

Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Rhode Island

Scientific Associate Director - Safety Pharmacology

**Join Amgens Mission of Serving Patients**

At Amgen, if you feel like youre part of something bigger, its because you are. Our shared missionto serve patients living with serious illnessesdrives all that we do.

Since 1980, weve helped pioneer the world of biotech in our fight against the worlds toughest diseases. With our focus on four therapeutic areas Oncology, Inflammation, General Medicine, and Rare Disease we reach millions of patients each year. As a member of the Amgen team, youll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.

Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, youll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

**Scientific Associate Director Safety Pharmacology**

**What you will do**

Lets do this. Lets change the world. The Scientific Associate Director will lead safety pharmacology lab-based activities within the Safety Pharmacology Sciences team and contribute directly to the success of Translational Safety & Risk Sciences (TSRS), the department responsible for nonclinical safety evaluation within Amgen Research. This role reports to the Senior Director of Safety Pharmacology Sciences.

This leadership role has multiple components: management of in vitro cardiac safety and electrophysiology laboratory and staff; lead and coordinate safety issue resolution studies (in vitro; in vivo); serve as a Safety Pharmacology Subject Matter Expert (SME) on project teams; and contribute to external scientific initiatives. The role requires integration of data across multiple assay systems and modalities to support candidate selection, risk assessment, clinical translation, regulatory strategy, and advancement of industry best practices.

**Key Responsibilities**

**1. Laboratory Leadership & Talant Management**

- Oversee the cardiac safety and electrophysiology laboratory, a core function responsible for ion channel, hiPSC-derived cardiomyocyte, and isolated heart assays.
- Manage exploratory and GLP-compliant studies, including outsourcing, protocol development, data review, and report finalization.
- Supervise scientific staff, promote their development and ensure high-quality timely data generation, study tracking, QC, reporting and stakeholder communication
- Maintain compliance with data integrity, safety, and environmental standards.
- Interface with internal & external partners to establish qualified NAMs models for safety assessment.

**2. Safety Pharmacology Subject Matter Expert (SME) on TSRS Teams**

- Provide expertise to support discovery and development programs and partner with TSRS project team representative (PTR) and other team members (PKDM, pathology, etc) to ensure aligned and efficient execution of safety strategies
- Ensure appropriate evaluation of target- and off target-based safety risks for diverse drug modalities in accordance with evolving ICH guidelines (S7A, S7B/E14, etc.).
- Guide study design, data interpretation, and next-step recommendations to support both lead optimization and clinical candidate selection and contribute to regulatory filings or inquiries.
- Provide oversight of safety pharmacology strategy across modalities, including small molecules, biologics, and emerging therapeutic approaches
- Coordinate investigative studies (e.g. human primary tissue acquisition, functional studies, etc.) and partner with internal and external (CRO) labs to execute.
- Collaborate with relevant experts to evaluate and integrate in vitro and in silico approaches.

**3. External Scientific Influence**

- Build and maintain external collaborations with academic, industry, and consortium partners to advance mechanistic safety understanding and safety pharmacology best practices
- Develop scientific eminence through peer-reviewed publications, presentations, and invited talks
- Promote adoption of human-relevant in vitro models (e.g., stem cellderived cardiomyocytes and other NAMs)
- Contribute to industry thinking on emerging modality-specific safety considerations (e.g., oligonucleotides and novel therapeutics)

**What we expect of you**

We are all different, yet we all use our unique contributions to serve patients. The dynamic professional we seek is a leader with these qualifications.

**Basic Qualifications:**

Doctorate degree \[and relevant post-doc where applicable\] and 4 years of relevant scientific experience

OR

Masters degree and 7 years of relevant scientific experience

OR

Bachelors degree and 9 years of relevant scientific experience

**Preferred Qualifications:**

- PhD in Pharmacology, Neuroscience, Physiology, Biomedical Sciences, or related field
- Broad experience in in vitro and or in vivo safety pharmacology across cardiovascular, respiratory and CNS domains
- Working knowledge of cardiac ion channel assays (e.g., hERG, Nav1.5, Cav1.2) and hiPSC-derived cardiomyocyte and isolated heart assays
- Experience managing outsourced studies and CRO relationships
- Experience supporting discovery and development project teams as a safety pharmacology SME or toxicology representative.
- Familiarity with GLP-enabling safety pharmacology packages and integration with toxicology studies
- Demonstrated people leadership and laboratory management experience
- Strong cross-functional communication and problem-solving skills
- Track record of scientific publications and participation in external scientific forums or consortia

**What you can expect of us**

As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, well support your journey every step of the way.

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.

In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:

- A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
- A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
- Stock-based long-term incentives
- Award-winning time-off plans
- Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.

**Apply now and make a lasting impact with the Amgen team.**

**careers.amgen.com**

In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.

**Application deadline**

Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.

**Sponsorship**

Sponsorship for this role is not guaranteed.

As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.

Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Director, Strategic Planning & Operations

**Join Amgens Mission of Serving Patients**

At Amgen, if you feel like youre part of something bigger, its because you are. Our shared missionto serve patients living with serious illnessesdrives all that we do.

Since 1980, weve helped pioneer the world of biotech in our fight against the worlds toughest diseases. With our focus on four therapeutic areas Oncology, Inflammation, General Medicine, and Rare Disease we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, youll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.

Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, youll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

**Director, Strategic Planning & Operations**

**Live**

**What you will do**

Lets do this. Lets change the world. In this vital role, the Director, Strategic Planning & Operations (SPO) for Amgens Bone Health Business Unit (BHBU) will ensure the effective operation of the U.S. Bone Health business while leading strategic initiatives critical to its growth and evolution.

The SPO will report directly to the VP/GM, BHBU, and work closely with the BHBU Leadership Team (LT), Marketing, Sales, and cross-functional partners, including Market Access, Medical, Finance, Business Insights, Patient Services, Regulatory, Supply, and Global colleagues.

This role serves as a strategic partner and integratorsupporting the BHBU operating rhythm; driving strategic planning, performance management, and governance; and ensuring business priorities are aligned and executed. The SPO will provide direct operational support to the VP/GM and BHBU LT, manage key business processes, and enable effective collaboration across functions.

In addition to core SPO responsibilities, the Director will lead strategic cross-functional projects that advance BHBU capabilities and performance, including AI adoption, operating-model evolution, commercial transformation, and improved ways of working.

This position provides an outstanding opportunity to work with senior commercial leaders, gain broad visibility into the U.S. Bone Health business, and directly contribute to strategies and operating practices that deliver value for patients.

**Responsibilities Include:**

**Strategic Planning and Operations Support**

- Provide strategic and operational leadership for BHBU, ensuring effective planning, prioritization, and coordination across Marketing, Sales, and cross-functional partners.
- Partner with the VP/GM and BHBU LT to support decision-making, execution, and alignment on key business priorities.
- Lead and coordinate annual and long-range planning processes, ensuring alignment across strategic priorities, plans, and milestones.
- Manage the BHBU operating cadence and key forums, including LT meetings, business reviews, business-planning meetings, and town halls.
- Drive performance-management processes, including business reporting, insights, and action planning to enable timely decisions and course correction.
- Facilitate MarketingSales integration, ensuring alignment between brand strategy, field execution, customer insights, and commercial priorities.
- Develop key presentations, reports, and communications for governance meetings, leadership forums, and planning sessions.
- Interface with Global partners to support appropriate alignment and information sharing.

**Leadership of Strategic Projects**

- Lead cross-functional strategic projects that advance the BHBU commercial strategy, operating model, and long-term performance.
- Drive adoption of AI tools and capabilities to enhance business efficiency, analytics, and decision-making.
- Identify and execute opportunities to strengthen cross-functional integration, agility, and execution through innovation and best practices.
- Lead transformation initiatives that improve business processes, collaboration, and ways of working.
- Translate strategic priorities into integrated plans, clear accountabilities, and measurable outcomes.
- Anticipate emerging business needs and recommend solutions that improve planning and execution.

**Win**

**What we expect of you**

We are all different, yet we all use our unique contributions to serve patients. The strategic professional we seek is a collaborative, commercially minded, and forward-thinking leader with these qualifications:

**Basic Qualifications:**

- Masters degree and 7 years of project management experience; OR
- Bachelors degree and 9 years of project management experience; AND
- 4 years of leadership experience leading teams, projects, programs, or directing the allocation of resources.

**Preferred Qualifications:**

- Commercial biopharmaceutical experience, with demonstrated partnership across Marketing, Sales, and cross-functional teams.
- Marketing experience, preferably at the Director level or with comparable strategic scope.
- Experience in Bone Health, osteoporosis, or a relevant specialty therapeutic area.
- Experience in sales leadership, launch excellence, lifecycle management, commercial planning, or performance management.
- Experience in management consulting, strategic planning, or commercial operations is a plus.
- Experience leading transformation initiatives and applying new tools, technologies, or operating models.
- Ability to lead complex initiatives through influence in a matrixed environment.
- Strong leadership, communication, stakeholder-management, and presentation skills.
- Demonstrated creativity and foresight in anticipating and solving complex business issues.

**Thrive**

**What you can expect from us**

As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, well support your journey every step of the way.

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.

In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:

- A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
- A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
- Stock-based long-term incentives
- Award-winning time-off plans and bi-annual company-wide shutdowns
- Flexible work models, including remote and hybrid work arrangements, where possible

**Apply now for a career that defies imagination**

**careers.amgen.com**

In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.

Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.

Sponsorship for this role is not guaranteed.

As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.

Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

Senior Associate Manufacturing - Electronic Batch Record Support (Multiple Positions)

**HOW MIGHT YOU DEFY IMAGINATION?**

Youve worked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills, experience and passion to work toward your goals? At Amgen, our shared missionto serve patientsdrives all that we do. It is key to our becoming one of the worlds leading biotechnology companies, reaching over 10 million patients worldwide. Come do your best work alongside other innovative, driven professionals in this meaningful role.

Be part of Amgen's newest and most advanced drug substance manufacturing plant. When completed, the Amgen FleX Batch facility will combine the latest in disposable technologies with traditional stainless-steel equipment to allow for maximum flexibility in operations. The FleX Batch facility will not only feature the best in-class drug substance manufacturing technologies with embedded industry 4.0 capabilities, but it will also integrate sustainability innovations to reduce carbon and waste, as part of Amgen's plan to be a carbon-neutral company by 2027.

**Senior Associate Manufacturing - Electronic Batch Record Support (Multiple Positions)**

**Live**

**What you will do**

Lets do this! Lets change the world! In this vital role, you will have the outstanding opportunity to support the start-up of the Amgen North Carolina (ANC) manufacturing facility. This is a manufacturing support role responsible for the generation of electronic documentation, for tracking of EBR metrics and for communication between the operations teams and the various functional groups working through start-up activities. During start up, Manufacturing Senior Associates will have oversight of electronic batch records operational readiness activities in multiple manufacturing areas such as: Dispensing, Buffer/Media Preparation, Upstream Cell Culture, Harvest, Downstream Purification, Analytical Testing, and Column Packing. Manufacturing Senior Associates can also support Standard Operating Procedure (SOP) creation, review, and approval; design of job aids and work instructions, advancement of digital tools to support manufacturing operations, and training of staff.

Job scope and responsibilities:

- Manufacturing support focused on Electronic Batch Record (EBR) generation using PAS-X (Korber), editing, real-time troubleshooting and managing the EBR validation for new or modified processes.

- Assist in the implementation of new MES integrations and functionalities.

- Support manufacturing in the troubleshooting and execution of EBRs

- Create and maintain Electronic Batch Records

- Support optimization of EBRs to improve functionality and align with process requirements

- Contribute to Lean Transformation through recording EBR metrics and application of continuous improvement tools.

- Participate and contribute to projects to introduce new products and/or advancement of new manufacturing technologies into the plant.

**Win**

**What we expect of you**

We are all different, yet we all use our unique contributions to serve patients. The dedicated professional we seek is a collaborative team player with these qualifications.

**Basic Qualifications:**

- High School/GED and 4 years of manufacturing or operations work experience**OR**

- Associates Degree and 2 years of manufacturing or operations work experience**OR**

- Bachelors Degree and 6 months of manufacturing or operations work experience**OR**

- Masters Degree

**Preferred Qualifications:**

- Completion of NC BioWorks Certification Program.

- Experience in biotechnology or pharmaceutical plant start up.

- Knowledge and process experience within a cGMP manufacturing facility or other highly regulated environment.

- Technical understanding of upstream and/or downstream manufacturing within a biotechnology production operation.

- Excellent verbal and written communication (technical) skills.

- Proficient Microsoft Office skills, and knowledge of other electronic systems such as SAP, EBR/MES, Delta V, and Electronic Quality Systems.

- Experience with PAS X (Korber) or comparable software for electronic batch records with some understanding of editing and validation.

**Thrive**

**What you can expect of us**

As we work to develop treatments that take care of others, we also work to care for our teammates professional and personal growth and well-being.

In addition to the base salary, Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including:

- Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.

- A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan

- Stock-based long-term incentives

- Award-winning time-off plans and bi-annual company-wide shutdowns

- Flexible work models, including remote work arrangements, where possible

**Apply now**

**for a career that defies imagination**

Objects in your future are closer than they appear. Join us.

**careers.amgen.com**

Lab Operations Manager

**Join Amgens Mission of Serving Patients**

At Amgen, if you feel like youre part of something bigger, its because you are. Our shared missionto serve patients living with serious illnessesdrives all that we do.

Since 1980, weve helped pioneer the world of biotech in our fight against the worlds toughest diseases. With our focus on four therapeutic areas Oncology, Inflammation, General Medicine, and Rare Disease we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, youll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.

Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, youll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

**Lab Operations Manager**

**What you will do**

Lets do this. Lets change the world. In this vital role you will support Amgen sponsored clinical trials, focusing on the laboratory category. In this key role, you will help us deliver on priority initiatives as well as provide strategic support to our study teams and key partners to optimize clinical trial implementation with our suppliers. The highest quality will be achieved by partnering effectively with our suppliers and providing robust supplier oversight with a fit for purpose governance program. Our scope is global and supports our clinical trials around the world. Come join an exceptional team that delivers for our study teams and our patients! Potentially up to 20% travel domestic and/or international.

- Provide guidance and input on technical and operational aspects of study design and execution
- Provide support and guidance during study startup and conduct with suppliers including activities such as sourcing, budget review, supplier selection, and scope of work development
- Develop strong global relationships with key stakeholders and suppliers
- Drive and facilitate the governance of laboratory suppliers
- Lead evaluation and qualification process of suppliers and advise partners on their selection
- Support the development and implementation of standards and processes for evaluation, qualification, selection, management, and monitoring of labs
- Provide oversight of technical and operational performance of laboratory suppliers across studies and manage escalated issues to resolution
- Support clinical trials and cross functional alignment with stakeholders, suppliers and partners for companion diagnostics development
- Participate on key initiatives and task forces with Therapeutic Areas, Early Development and Research
- Share expertise in emerging technologies through company interactions, literature, and industry conferences
- Contribute to the continuous improvement of Supplier Governance and the wider GDO organization and support the integration activities for Amgen acquisitions, as appropriate

**What we expect of you**

We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a person with these qualifications.

**Basic Qualifications:**

- Doctorate degree
  OR
- Masters degree and 2 years of lab and clinical trials experience
  OR
- Bachelors degree and 4 years of lab and clinical trials experience
  OR
- Associates degree and 8 years of lab and clinical trials experience
  OR
- High school diploma / GED and 10 years of lab and clinical trials experience

**Preferred Qualifications:**

- Strong laboratory background, including clinical testing, central laboratory operations, or laboratory-related project management experience.
- Solid understanding of laboratory workflows, procedures, and operational best practices.
- Knowledge of clinical trial processes and the role of laboratory operations within clinical research.
- Experience overseeing and managing laboratory studies, projects, or research initiatives.
- Ability to coordinate cross-functional teams and ensure timely execution of study deliverables.
- Familiarity with regulatory and quality requirements applicable to clinical and laboratory environments.

**What you can expect from us**

As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, well support your journey every step of the way.

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.

In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:

- A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
- A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
- Stock-based long-term incentives
- Award-winning time-off plans
- Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.

**Apply now and make a lasting impact with the Amgen team.**

**careers.amgen.com**

In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.

**Application deadline**

Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.

**Sponsorship**

Sponsorship for this role is not guaranteed.

As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.

Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

District of Columbia

Process Development Sr Scientist

**Join Amgens Mission of Serving Patients**

At Amgen, if you feel like youre part of something bigger, its because you are. Our shared missionto serve patients living with serious illnessesdrives all that we do.

Since 1980, weve helped pioneer the world of biotech in our fight against the worlds toughest diseases. With our focus on four therapeutic areas Oncology, Inflammation, General Medicine, and Rare Disease we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, youll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.

Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, youll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

**Process Development Sr Scientist**

**What you will do**

Lets do this. Lets change the world. In this vital role you will join the pivotal synthetic Attribute Sciences team, part of the integrated Pharmaceutical Attribute Sciences (iPAS) department, located in Thousand Oaks, CA. This team plays a crucial role in pivotal phase analytical development, including method development, validation, transfer, process and product development support, and GMP testing of drug substances and drug products.

The analytical scientist will work closely with a team of analysts and scientists responsible for the technical aspects of developing analytical tools to gain understanding of key quality attributes in product and process for late phase synthetic programs across small molecules, synthetic peptides, siRNA, and synthetic components of conjugates. The analytical scientist will integrate and optimally utilize platform and in-depth product attribute knowledge to advance Amgen products and ensure success through pivotal clinical phases to marketing authorization application.

**Key Responsibilities:**

- Define analytical control strategies and implement methodologies to support the development of late-phase clinical programs, with a strong ability to articulate the challenges and complexities associated with analytical control strategy development.
- Develop, optimize, authorize and validate analytical methods for attribute understanding and characterization across synthetic modalities, including small molecules, synthetic peptides, siRNA, and the synthetic components of antibodydrug conjugates.
- Collaborate closely with drug substance and drug product process development colleagues to achieve project objectives.
- Provide analytical data to support drug substance and drug product development, including purity analysis, chiral purity and structure elucidation using mass spectrometry.
- May lead activities and method transfer to contract manufacturing organization (CMO) or contract testing lab (CTL). Review and approve protocols, reports from CMO and CTL.
- Support project team lead to author technical reports and analytical Chemistry, Manufacturing and Controls (CMC) sections in regulatory documents.
- May lead and mentor a small group of scientists.

**What we expect of you**

We are all different, yet we all use our unique contributions to serve patients. The dynamic professional we seek is an individual with these qualifications.

**Basic Qualifications:**

- Doctorate degree PhD OR PharmD OR MD \[and relevant post-doc where applicable\]
  OR
- Masters degree and 3 years of Scientist experience
  OR
- Bachelors degree and 5 years of Scientist experience

**Preferred Qualifications:**

- PhD in Analytical Chemistry, Organic Chemistry, Physical Chemistry, Material Sciences, Pharmaceutical Sciences, or related discipline.
- 2+ years post-PhD experience in the pharmaceutical or biotech industry, focusing on process and product development, and analytical method development for drug substances and products.
- Experience in conjugates method development, characterization, and analytical control strategy especially having mass spectroscopy (MS) experience.
- Strong understanding of synthetic molecule analysis and structure elucidation informed by knowledge of organic chemistry.
- Hands on experience in method development, validation, and transfer for in-process, release, and stability testing
- Proficiency in a broad spectrum of structure elucidation and physicochemical techniques including MS, UV, NMR, FTIR, etc.
- Familiarity with USP monographs and chapters, and ICH/FDA guidance documents related to analytical method transfer and validation, impurities, mutagenic impurities, etc.
- Solid understanding of GLP and GMP requirements and their application in a phase appropriate manner
- Experience in technical transfer for non-GMP and GMP production and testing to external contract organizations, able to manage deliverables against timelines.
- Excellent communication skills and ability to provide cross-functional leadership and guidance to CMC and non-clinical teams, e.g. informing and defending the Quality Target Product Profile
- Ability to work effectively in cross-functional teams, and across various geographic locations in different time zones.
- Excellent technical writing skills with attention to detail in authoring methods, specifications, technical reports, and regulatory filing documents

**What you can expect of us**

As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, well support your journey every step of the way.

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.

In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:

- A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
- A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
- Stock-based long-term incentives
- Award-winning time-off plans
- Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.

**Apply now and make a lasting impact with the Amgen team.**

**careers.amgen.com**

In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.

**Application deadline**

Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.

**Sponsorship**

Sponsorship for this role is not guaranteed.

As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.

Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Associate Manufacturing - Nights (D shift)

**Join Amgens Mission of Serving Patients**

At Amgen, if you feel like youre part of something bigger, its because you are. Our shared missionto serve patients living with serious illnessesdrives all that we do.

Since 1980, weve helped pioneer the world of biotech in our fight against the worlds toughest diseases. With our focus on four therapeutic areas Oncology, Inflammation, General Medicine, and Rare Disease we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, youll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.

Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, youll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

**Associate Manufacturing - Nights**

**What you will do**

Lets do this. Lets change the world. In this vital role you will perform operations within the Manufacturing area, specifically solutions, at Amgen's innovative Rhode Island facility. You will be required to know, comprehend, and apply Good Manufacturing Practices (GMP), as well as understand, follow, and document in batch records.

Responsibilities Include:

- Perform batching and transfer of Buffers and Media in appropriate areas according to Standard Operating Procedures (SOPs).
- Follow and monitor critical processes, complete routine validation protocols, and regularly draft and revise documents such as Manufacturing Procedures, SOPs, and technical reports.
- Conduct basic troubleshooting and assist in the review of documentation for assigned functions.
- May also have the responsibility of initiating and owning area Deviations, revising SOP's and performing LEAN functions.
- Identify, recommend, and implement improvements related to routine functions.

In this role, you will be expected to work a 12-hour shift (7PM-7AM) on a rotating schedule (D- Shift). This includes extra benefits such as **receiving an added 15% shift differential.**  The schedule during the initial on-boarding/training phase (2-6 weeks) will be administrative (Monday through Friday, approximately 8am to 5pm).

**What we expect of you**

We are all different, yet we all use our unique contributions to serve patients. The driven professional we seek is a self-starter with these qualifications.

**Basic Qualifications:**

- High school/GED + 2 years of manufacturing or operations work experience OR
- Associates + 6 months of manufacturing or operations work experience OR
- Bachelors Degree in a related field

**Preferred Qualifications:**

- Bachelors degree in Science or Engineering
- Knowledge of large-scale biotechnology operations such as purification, cell culture, aseptic processing, etc.
- Knowledge of Single-use-Systems
- CFR and Regulatory knowledge
- Mechanical ability/expertise
- Basic statistical mathematical skills
- Ability to interpret and apply GMP knowledge
- Understanding of analytical methods for manufacturing area
- Demonstrated technical writing capability
- Able to demonstrate project management skills and presentation skills
- Ability to understand, apply and evaluate basic chemistry, biology and physical principles
- Basic troubleshooting skills on production equipment
- Experience with Delta V
- Experience with lab equipment/testing

**What you can expect of us**

As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, well support your journey every step of the way.

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.

In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:

- A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
- A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
- Stock-based long-term incentives
- Award-winning time-off plans
- Flexible work models, including remote and hybrid work arrangements, where possible

**Apply now and make a lasting impact with the Amgen team.**

**careers.amgen.com**

In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.

**Application deadline**

Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.

**Sponsorship**

Sponsorship for this role is not guaranteed.

As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.

Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Executive Director, Global Site & Study Operations, Americas

**Join Amgens Mission of Serving Patients**

At Amgen, if you feel like youre part of something bigger, its because you are. Our shared missionto serve patients living with serious illnessesdrives all that we do.

Since 1980, weve helped pioneer the world of biotech in our fight against the worlds toughest diseases. With our focus on four therapeutic areas Oncology, Inflammation, General Medicine, and Rare Disease we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions.

As a member of the Amgen team, youll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.

Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, youll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

**Executive Director, Global Site Study Operations, Americas**

**What you will do**

Lets do this. Lets change the world. In this vital role as Executive Director, Global Site Study Operations, America you will be accountable for regional Study & Site Operations leadership across the Americas clinical trial portfolio. This role provides enterprise-level strategic direction, operational oversight, people leadership, and cross-functional influence to ensure high-quality, timely, compliant, and predictable trial delivery. The role leads regional and country/hub leaders, shapes site engagement and monitoring strategies, and represents the region in global governance and portfolio decision-making forums.

**Key Responsibilities**

- Oversees countries and regions within the Americas including US, Canda, and LATAM.
- Operates at an enterprise leadership level and is expected to combine portfolio-level strategic leadership, operational accountability, people leadership, and cross-functional influence.
- Initiation, management, quality, and completion of Phase I-IV clinical trials in the region, ensuring timely, high-quality delivery in compliance with ICH-GCP, regulatory requirements, and company policies.
- Guiding the organization on modern site-monitoring approaches and associated resource strategies.
- Represent the region and/or GSSO in enterprise forums, providing insights that inform portfolio, program, and study-planning decisions
- Build and develop a high-performing Country/Hub head team as strategic leaders, creating a culture of accountability, innovation, and operational excellence in their regions.
- Champion innovation and continuous improvement in start-up approaches, embedding digital solutions, predictive analytics, and harmonized ways of working across the global portfolio.

**Leadership and Delivery**

- Accountable for implementing the Regional Study & Site Operations strategy ensuring that study resources are appropriately allocated according to global operations and priorities.
- Optimize deployment of resources, including internal and staff augmented, across clinical programs.
- Interpret and cascade GDO strategies into consistent regional andcountry-level delivery of studies, site engagement, and monitoring against quality standards, and other cross-functional processes and initiatives, balancing standardization with local/regional adaptability.
- Provide executive oversight of high-risk or strategically important clinical programs.
- Act as the GSSO escalation point for study risks and issues, coaching teams through mitigation strategies and scenario planning, ensuring timely resolution and visibility.
- Build and sustain a CRA monitoring organization, including resourcing strategies and portfolio considerations, while ensuring monitoring standards and organizational capabilities are in place.
  - Ensure monitoring strategies incorporate, in partnership with relevant cross-functional capabilities, the appropriate use of centralized monitoring, on-site and remote monitoring, targeted SDR/SDV, and risk/quality indicators and thresholds.

- Lead through an evolving site engagement model, executing strategies that strengthen relationships with clinical research sites, improve site experience, and enhance site performance across clinical development programs.
- Holds decision-making authority for all study and site operations in the region, including resource allocation, budget utilization, and vendor performance.
- Maintain oversight of the regional clinical trial portfolio, including study start-up, enrollment, execution, database lock, and study closeout. Coach and mentor teams in management of challenges and issue escalation.
- Ensure appropriate inspection readiness throughout the clinical trial lifecycle and follow through to audits and inspections in the region.
- Represents GSSO and/or the region in global governance bodies with delegated authority to influence portfolio decisions, timelines, and resourcing.

**Capability Building & People Leadership**

- Lead, coach, and develop regional and country Study & Site Operations leaders, including performance management, succession planning, and leadership bench development.
- Build the organizational capabilities, resourcing, and operating model needed to meet current and future regional portfolio requirements.
- Foster a high-performing, inclusive, accountable, and patient-focused culture across geographically distributed teams.
- Lead organizational changes and enable adoption of new operating models, technologies, monitoring approaches, and clinical development practices.
- Foster a culture of accountability, collaboration, inclusion, quality, continuous improvement, and patient focus.
- Lead organizational change and support adoption of new operating models, technologies, and clinical development approaches.

**Operational Excellence & Cross-Functional Engagement**

- Lead, coach, and develop regional and country Study & Site Operations leaders, including performance management, succession planning, and leadership bench development.
- Build the organizational capabilities, resourcing, and operating model needed to meet current and future regional portfolio requirements.
- Foster a high-performing, inclusive, accountable, and patient-focused culture across geographically distributed teams.
- Lead organizational changes and enable adoption of new operating models, technologies, monitoring approaches, and clinical development practices.
- Identify opportunities to simplify processes, improve productivity, and increase predictability of clinical trial delivery.
- Use data and performance insights to drive decisions and continuous improvement.
- Lead or sponsor regional and global clinical operations transformation initiatives.
- Embed a center of excellence mindset, encouraging knowledge-sharing and best practice adoption globally.

**Stakeholder Engagement & Influence**

- Partner with leaders across Clinical Development, Operations, Regulatory, and Regions to ensure study start-up strategy enables trial success, and resources required to execute are assigned and aligned to GSSO. Maintain and strengthen cross-functional and global business relationships, representing GSSO.
- Act as a visible change leader, promoting GSSO as a strategic enabler of faster, more predictable clinical trial execution and drive cross-functional sponsorship.
- Cultivate leadership and capability across geographies to build resilient, empowered teams that consistently deliver results.

**Authority**

- Accountable for regional level oversight and delivery of clinical trials.
- Holds line management authority for regional and country operations leaders, including performance management, talent development, succession planning, and capability building.
- Sets regional delivery goals, operating expectations, and performance standards across study start-up, site engagement, monitoring, execution, and closeout.
- Capability build, talent and performance management, and acting as a liaison for cultural differences within region.

**Outputs**

- Successful and timely trial delivery across the region with inspection-ready quality.
- Cohesive and aligned execution across countries, with consistent quality and compliance.
- Sustained regionalinvestigator and site engagement enabled through consistent country/hub-level engagement strategies driving strong patient recruitment and retention.
- High-performing regional team with strong leadership, empowered Country Heads acting as effective strategic representatives in their geographies.

**Competencies**

- Adept at navigating cross-geographic and cultural dynamics and leading efficient global teams. Demonstrated ability to motivate geographically dispersed teams inclusively and drive strategy and execution.
- Experience in delivering portfolio/cross-study level, budgets, timelines, and performance metrics (time, cost, quality) aligned to global / functional priorities.
- Collaborate with global and regional leadership to ensure effective country and site strategies guiding study start up, inspection, and delivery.
- Proficient in overseeing resource and budget allocation in accordance with functional financial principles, ensuring optimal resource planning aligned with global clinical priorities.
- Experience in assessing internal capabilities and identifying key capabilities, proficient in driving and leading continuous improvement initiatives for team's working practices, ensuring cross-functional adoption of new processes.
- Experience leading organizations through cross-functional change initiatives, including identifying solutions to complex problems, driving innovation, and evolving strategies and structures to meet future business needs.
- Proven ability to foster impactful cross-functional collaboration through exceptional communication and influence.
- Enterprise, pro-active thinking with the ability to assess broad impacts across multiple product portfolios to identify innovative solutions.
- Build strong partnerships with Clinical Development, Medical, Regulatory Affairs, Safety, Biometrics, Data Management, Clinical Supply, Quality, and other functions.
- Communicate portfolio performance, risks, and strategic recommendations clearly to senior leadership.

**What we expect of you**

We are all different, yet we all use our unique contributions to serve patients. The executive candidate we seek is an experienced leader with the following qualifications.

**Basic Qualifications:**

- Doctorate degree & 6 years of global site study experiences OR
- Masters degree & 10 years of global site study experiences OR
- Bachelors degree & 12 years of global site study experiences AND
- 6 years of managerial experience directly managing people and/or leadership experience leading teams, projects, programs or directing the allocation of resources

**Preferred Qualifications:**

- Bachelor's degree in life sciences, pharmacy, nursing, medicine, or a related discipline required; advanced degree preferred.
- 15+ years of progressive experience in pharmaceutical, biotechnology, CRO, or clinical research organizations.
- Extensive clinical operations and study management experience across multiple phases of clinical development.
- Significant leadership experience managing managers and/or large, geographically distributed clinical operations organizations, inclusive of a monitoring organization.
- Demonstrated experience overseeing complex global or regional clinical trial portfolios.
- Demonstrated experience with CRO/vendor governance, outsourcing models, budget management, and resource planning.
- Track record of leading organizational change and improving clinical operations performance.
- Strong knowledge of ICH-GCP, clinical development processes, and applicable regulatory requirements. Experience supporting regulatory inspections and clinical quality management.
- Experience working for or overseeing clinical research vendors (CROs, central laboratories, imaging vendors, etc.
- Experience managing clinical operations across relevant geography / region, including strong understanding of local regulatory requirements around clinical trials.

They will also embody the Amgen leadership attributes which are:

- **Inspire:**  Create a connected, inclusive, and inspiring work environment that empowers talent to thrive
- **Accelerate:**  Enable speed that matches the urgency of patient needs by encouraging progress over perfection
- **Integrate:**  Connect the dots to amplify the collective power of Amgen to drive results for patients, staff, and shareholders
- **Adapt:**  Lead through change by adapting to an ever-changing environment and defining a clear course of action to deliver results

**What you can expect of us**

As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, well support your journey every step of the way.

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is $263,760 - $356,852. Actual salary will vary based on several factors including, but not limited to, relevant skills, experience, and qualifications.

In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:

- Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.
- A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
- Stock-based long-term incentives
- Award-winning time-off plans and bi-annual company-wide shutdowns
- Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.

Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.

Sponsorship for this role is not guaranteed.

As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.

Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Process Development Senior Associate

**Join Amgens Mission of Serving Patients**

At Amgen, if you feel like youre part of something bigger, its because you are. Our shared missionto serve patients living with serious illnessesdrives all that we do.

Since 1980, weve helped pioneer the world of biotech in our fight against the worlds toughest diseases. With our focus on four therapeutic areas Oncology, Inflammation, General Medicine, and Rare Disease we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, youll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.

Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, youll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

**Process Development Senior Associate**

**What you will do**

Lets do this. Lets change the world. In this vital role you will join Amgens DSTS group within Process Development (PD) is responsible for the invention, development, and implementation of drug substance manufacturing processes and technologies to advance Amgen's exciting portfolio of synthetic and hybrid assets.

Amgen is currently seeking a talented Process Development Senior Associate to join our Drug Substance Technologies - Synthetics (DSTS) group in Thousand Oaks, California. Senior Associates in our team collaborate with chemists, process engineers, and attribute scientists to support drug substance development and manufacturing from early to late-stage development. The successful candidate will be a highly motivated and team-oriented individual with prior lab-based research experience in bioconjugation.

- Work within a drug substance team comprised of chemists, engineers, and attribute scientists to solve technical problems
- Contribute to the development of safe, robust, and cost-effective processes to manufacture synthetic and hybrid drug substances
- Support cGMP manufacturing and technology transfer to our internal manufacturing facilities and external contract manufacturers
- Support process characterization activities, including process understanding and modeling
- Contribute to drug substance development teams by providing experimental results, technical updates, documentation, data interpretation, recommendations, etc.
- Works regularly with a supervisor to advance projects within required deadlines.
- Work cross-functionally to deliver regulatory documents and support regulatory filings
- Follows good laboratory documentation practices and standard operating procedures

**What we expect of you**

We are all different, yet we all use our unique contributions to serve patients. dynamic professional we seek is an individual with these qualifications.

**Basic Qualifications:**

- Masters degree
  OR
- Bachelors degree and 2 years of Scientific experience
  OR
- Associates degree and 4 years of Scientific experience
  OR
- High school diploma / GED and 6 years of Scientific experience

**Preferred Qualifications:**

- M.S. in organic chemistry or biochemistry/chemical biology with a specialization in bioconjugation chemistry
- Prior bioconjugation experience in the biopharmaceutical or pharmaceutical industry
- Demonstrated ability to work in a chemistry laboratory with minimal supervision
- Ability to independently collect and interpret analytical results (NMR, HPLC, MS, IR, Raman, etc)
- Excellent written and verbal communication skills, ability to multitask, effectively plan and follow through on projects
- A research summary included with CV is strongly encouraged

**What you can expect of us**

As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, well support your journey every step of the way.

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.

In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:

- A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
- A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
- Stock-based long-term incentives
- Award-winning time-off plans
- Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.

**Apply now and make a lasting impact with the Amgen team.**

**careers.amgen.com**

In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.

**Application deadline**

Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.

**Sponsorship**

Sponsorship for this role is not guaranteed.

As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.

Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Sr. Engineer, Process Development

**Join Amgens Mission of Serving Patients**

At Amgen, if you feel like youre part of something bigger, its because you are. Our shared missionto serve patients living with serious illnessesdrives all that we do.

Since 1980, weve helped pioneer the world of biotech in our fight against the worlds toughest diseases. With our focus on four therapeutic areas Oncology, Inflammation, General Medicine, and Rare Disease we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, youll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.

Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, youll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

**Sr Engineer**

**What you will do**

Lets do this. Lets change the world. In this vital role you will be responsible for authoring technical reports, leading risk assessments, and contributing to regulatory documents through all phases of technology transfer and commercialization.

Position located in either Cambridge, MA or Thousand Oaks, CA.

Domestic and International Travel: up to 20%

- Technical and lab-based execution of bench and kilogram-scale experimentation and process modeling & simulation to design and optimize robust synthetic and hybrid processes.
- Critical evaluation of novel chemical processes for the identification of process improvement opportunities and requirements necessary to ensure safe and successful scale-up and tech transfer.
- Design, optimize, and deploy process models for reaction kinetics, mass transfer, separations, distillations, isolations, drying, and relevant hydrodynamic operations.
- Model and analyze the economic value and environmental impact of process synthetic processes and manufacturing concepts.
- Initiate and complete standard practices for technology transfer of synthetic processes which include drafting process transfer documents, process fit assessments, manufacturing support, risk analysis and process documentation.
- Represent organization within a multi-functional team to ensure deliverables are aligned with tech transfer timeline, such that key milestones are established and achieved.
- Apply standard and advanced engineering techniques and procedures to provide solutions to a variety of technical chemical and process issues that will be encountered during process development, tech transfer and scale-up.
- Routinely monitor manufacturing processes for performance indicators and operations. Lead problem resolution and provide troubleshooting guidance.
- Apply engineering principles and statistical analysis, including design of experiments, in-order to critically evaluate chemical processes for identification of process improvements and requirements necessary for scale up and tech transfer.
- Author, review and/or approve of process documentation needed for process validation and commercialization activities.
- Contribute to key regulatory and quality activities such as NDAs, non-conformances, process performance qualification and continued process verification.
- Provide on-the-floor support to ensure successful scale-up and facilitate rapid problem solving and decision-making.
- Lead or represent department as subject matter expert for process risk analysis.
- Work closely with process development chemists, formulation scientists, and analytical chemists to generate and interpret data to provide improved understanding and guidance for synthesis and unit operations.

**What we expect of you**

We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a leader with these qualifications.

**Basic Qualifications:**

Doctorate degree

OR

Masters degree and 2 years of **Engineering Experience**

OR

Bachelors degree and 4 years of **Engineering Experience**

OR

Associates degree and 8 years of **Engineering Experience**

OR

High school diploma / GED and 10 years of **Engineering Experience**

**Preferred Qualifications:**

- Familiar with bioprocessing unit operations required to support ADCs and/or oligonucleotides, including conjugation and purification.
- Experience in developing and executing experimental plans to evaluate and develop processes to achieve optimum cost, robustness, and productivity.
- Experience related to technology transfer, scale-up and manufacturing of synthetic molecules in a regulated environment. This includes technical support for non-conformance investigations and other commercial support activities.
- Experience authoring regulatory documents for commercialization of drug substance processes: CMC Module 3, RTQs, and annual reports.
- Experience building and utilizing first-principles models (e.g., reaction kinetics, mass transfer, separations, distillations, isolations, drying, and hydrodynamics) with proficiency across several modeling platforms.
- Knowledge of analytical techniques and solid-state characterization with fluency in a wide variety of methods including HPLC, GC, MS, NMR, FTIR, LOD, TOC, FBRM, particle size determination, etc.
- Experience using data science and/or advanced statistical analysis to solve processing issues and evaluate opportunities for process improvements.
- Proficient understanding of regulatory and cGMP requirements.
- Command of lab and plant operations and associated safety practices.
- Familiarity with HPAPI processing and containment. Engineering knowledge around linker payload chemistry and scale-up.
- Strong communication and presentation skills

**What you can expect from us**

As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, well support your journey every step of the way.

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.

In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:

- A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
- A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
- Stock-based long-term incentives
- Award-winning time-off plans
- Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.

**Apply now and make a lasting impact with the Amgen team.**

**careers.amgen.com**

In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.

**Application deadline**

Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.

**Sponsorship**

Sponsorship for this role is not guaranteed.

As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.

Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

Undergrad Intern - Operations Engineering (Summer 2027)

**Join Amgens Mission of Serving Patients**

At Amgen, if you feel like youre part of something bigger, its because you are. Our shared missionto serve patients living with serious illnessesdrives all that we do.

Since 1980, weve helped pioneer the world of biotech in our fight against the worlds toughest diseases. With our focus on four therapeutic areas Oncology, Inflammation, General Medicine, and Rare Disease we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity-related conditions. As a member of the Amgen team, youll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.

Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, youll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

**Undergrad Intern - Operations Engineering (Summer 2027)**

**What You Will Do**

Lets do this. Lets change the world. This approximately 13 week remote (or onsite at either New Albany, Ohio; Holly Springs, North Carolina; South San Francisco, California; or Thousand Oaks, California) internship program offers meaningful project and operational experiences with the worlds leading biotechnology company. During this program, you will work closely with a team of Amgens Engineers that support one of the following areas:

- Engineering Technical Authority
- Global Capital Project Management
- Project Controls and Strategy
- Engineering Operations Services
- Environment, Health & Safety

**Key responsibilities include:**

- Partner with project design teams and subject-matter experts to support engineering project development, plans, standards, equipment selection, and technical documentation.
- Support engineering assessments, technical feasibility evaluations, lifecycle impact assessments, cost analyses, and project business cases.
- Research project scopes, construction and engineering processes, and emerging technologies to identify improvement opportunities.
- Support the development and implementation of strategic Engineering projects, including capital planning and project controls activities.
- Help develop, test, or improve digital, automation, data, or AI-enabled tools that streamline business processes and advance operational efficiency.
- Contribute to safety, health, and environmental initiatives that improve compliance, reduce operational risk, and support workforce well-being.
- Communicate findings, recommendations, and project updates to Engineering and cross-functional stakeholders.

**Program Eligibility Requirements**

- Expected completion of one year of study from an accredited college or university prior to the internship commencing
- Expected continued enrollment in an accredited college or university following the internship program
- Student must be located in the United States for the duration of the internship program
- Must be available to work a full-time schedule.

**What We Expect of You**

We are all different, yet we all use our unique contributions to serve patients. The Engineering undergraduate intern we seek is a collaborative team-player that exemplifies the following qualifications:

**Basic Qualifications:**

Amgen requires that all individuals applying for an undergrad internship or a co-op assignment at Amgen must meet the following criteria:

- 18 years or older
- Currently enrolled in a full-time Bachelors Degree program from an accredited college or university with a 3.0 minimum GPA or equivalent

**Preferred Qualifications**

- Degree concentration(s) in one of the following areas:
- **Engineering, project delivery, or construction:**  Chemical, Mechanical, Biomedical, Electrical, Industrial, Civil, Construction, Environmental, or Systems Engineering; Construction Management; Architecture; Design and Drafting Technology; or Engineering Technology
- **Digital, data, and AI:**  Computer Science, Data Science, Artificial Intelligence, Machine Learning, Information Systems, Analytics, Mathematics, Statistics, or a related technical field
- **Environment, health, and safety:**  Environmental or Occupational Health, Environmental Science, Public Health, Toxicology, Nursing, Biomechanics/Ergonomics, or a related field

- Interest in applying engineering principles, data, AI, automation, and continuous-improvement methods to support project justification, design, development, capital planning, safety, or operational excellence
- Familiarity with Microsoft Office applications, including Excel and PowerPoint.
- Exposure to data analysis, visualization, Python, SQL, Power BI, BIM/Revit, automation, or generative AI tools are preferred
- Strong written and verbal communication, relationship-building, and problem-solving skills
- Ability to manage time effectively, work independently when needed, and collaborate in a matrixed environment
- Demonstrated curiosity, initiative, and ability to translate technical information into clear recommendations

**What You Can Expect of Us**

As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, well support your journey every step of the way.

The base pay range for this opportunity in the U.S. is $28.87 per hour.

- Build a network of colleagues that will endure and grow throughout your time with us and beyond.
- Bring your authentic self to the table and become the professional youre inspired to be through accepting a culture that values the diversity of thought and experience and will flex to your strengths and possibilities.
- Participate in executive and social networking events, as well as community volunteer projects.

**Apply now and make a lasting impact with the Amgen team.**

**careers.amgen.com** Please search for Keyword R-255335

In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.

**Application deadline**

Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.

**Sponsorship**

Candidates must be authorized to work in the U.S. for the duration of this program. Sponsorship for future FTE roles is not guaranteed.

As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.

Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Principal Manufacturing Systems Engineer Upstream/Downstream Process Automation

**HOW MIGHT**YOU**DEFY IMAGINATION?**

Youveworked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills,experience,and passion to work toward your goals? At Amgen, our shared missionto serve patientsdrives all that we do. It is key to our becoming one of the worlds leading biotechnology companies, reaching over10 million patientsworldwide. Come do your best work alongside other innovative, driven professionals in this meaningful role.

Be part of Amgen's newest and most advanced drug substance manufacturing plant. When completed, the AmgenFleXBatch facility will combine the latest in disposable technologies with traditional stainless-steel equipment to allow for maximum flexibility in operations. TheFleXBatch facility will not only feature the best in-class drug substance manufacturing technologies with embedded industry 4.0 capabilities, but it will also integrate sustainability innovations to reduce carbon and waste, as part of Amgen's plan to be a carbon-neutral company by 2027.

**Principal Manufacturing Systems Engineer Upstream/Downstream Process Automation**

**What you will do**

Lets do this! Lets change the world! In this vital role, you will serve as a subject matter expert in automation engineering, driving innovation, solving complex challenges, and influencing the design and implementation of automation systems for upstream and downstream bioprocessing. You will collaborate across engineering, manufacturing, and quality teams to ensure robust, compliant, and scalable automation solutions that support 24/7 operations.

The Principal Manufacturing Systems Engineer will join the Facilities & Engineering (F&E) group. This role will partner closely with the corporate engineering team during the design, build, commissioning, and qualification phases and later transitioning to supporting daily operations for drug substance production. This role will be instrumental in developing automation domain expertise and supporting operational readiness.

Job responsibilities include:

- **Site design, construction, start-up, and operational readiness:**
  - Support design reviews while partnering closely with the corporate engineering team to represent site interests and requirements.
  - Execute and support the commissioning and qualification of process equipment automation in alignment with GMP requirements, while working in partnership with global engineering during site installation. Ensure their operational capability is aligned with manufacturing requirements and GMP regulation and on-time project delivery.
  - Collaborate with the site process engineering team to understand key process requirements and develop process control automation solutions primarily utilizing Emerson DeltaV Distributed Control System (DCS).
  - Lead commissioning and qualification efforts, including Automation Installation Verification/Automation Check Out (IV/ACO), ensuring compliance with GMP and project timelines.
  - Partner with various organizational units to support tasks including operational readiness, document reviews, deviation investigation and change controls.
  - Provide mentoring to develop and accelerate site technical automation capabilities.
- **Site Operations:**
  - Act as responsible system owner for automation systems, providing day-to-day automation support including 24 x 7 onsite/on-call support, troubleshooting, and daily automation team meetings.
  - Provide technical leadership to troubleshoot, identify and resolve process and system issues as needed.
  - Effectively collaborate with key customers and support groups (e.g. Manufacturing, Quality, Process Development, Maintenance, network partners).
  - Perform automation change assessments, implement automation system configuration changes, and support engineering and process qualification runs.
  - Lead continuous improvement initiatives including improvements to safety, reliability, efficiency, and sustainability, such as cycletimes, yields, and efficiency of unit operations in manufacturing.
  - Perform and maintain data integrity in accordance with the current Amgen and industry standards.
  - Serve as a technical mentor to junior engineers and cross-functional teams.
  - Influence automation strategy and standardization across the site and network.
  - Represent plant automation in Amgen global network forums related to automation and process control.
  - Represent automation during audits, and regulatory inspections.
  - Stay current with emerging technologies and industry trends to identify opportunities for innovation.
  - Provide strategic, tactical management, and leadership to ensure 24x7 day-to-day reliability of plant operations.
  - Up to 10% domestic/international travel

**What we expect of you**

We are all different, yet we all use our unique contributions to serve patients. The automation professional we seek enjoys challenges and is motivated to help serve patients with these qualifications.

Basic Qualifications:

- Doctorate degree and 2 years of engineering experience

OR

- Masters degree and 4 years of engineering experience

OR

- Bachelors degree and 6 years of engineering experience

OR

- Associates degree and 10 years of engineering experience

Or

- High school diploma / GED and 12 years of engineering experience

And

- 2 years of managerial experience directly managing people and/or leadership experience leading teams, projects, programs or directing the allocation of resources

Preferred Qualifications:

- Degree in Electrical Engineering, Computer Science, Chemical Engineering or Biotech Engineering.
- Extensive experience with Emerson DeltaV, Process Control Network design including network segregation, Process Control Systems: Virtual Infrastructure design and implementation, System Integration using OPC, Foundation Fieldbus, and Profibus.
- Hands-on experience with IO-Link technology for smart sensor/actuator integration in automated manufacturing environments.
- Familiarity with Process Analytical Technology (PAT) tools and strategies for real-time process monitoring and control in biopharmaceutical manufacturing.
- Direct knowledge of integrating various OEM automation software and field instrumentation technologies.
- In-depth knowledge of industry standards such as 21 CFR Part 11, ASTM 2500, S88, S95, GAMP, GDP, and GMP.
- Experience working in a regulated environment (e.g. cGMP, OSHA, EPA, etc.), experience interacting with regulatory agencies and inspectors, and familiarity with GMP quality systems/processes such as change control, non-conformances, corrective and preventative actions, and qualifications/validation
- Experience with Tech Transfer, Process Design, and Commissioning & Qualification.
- Deep understanding of biopharmaceutical manufacturing processes including Upstream (Seed train, production Bioreactors, Harvest), and Downstream Purification (e.g. Chromatography and viral Filtration skids, UFDF), and CIP/SIP Skids.
- Ability and willingness to mentor and develop engineering staff and embrace a team-based culture that relies on collaboration for effective decision-making.
- Strong leadership, technical writing, and communication/presentation skills.
- Proven ability to influence cross-functional teams and drive technical decisions.
- Work schedule flexibility as required to support 24/7 operations, requiring occasional after-hours engineering coverage

Principal Process Engineer - Upstream/Downstream

Job Description

**Join Amgens Mission of Serving Patients**

At Amgen, if you feel like youre part of something bigger, its because you are. Our shared missionto serve patients living with serious illnessesdrives all that we do.

Since 1980, weve helped pioneer the world of biotech in our fight against the worlds toughest diseases. With our focus on four therapeutic areas Oncology, Inflammation, General Medicine, and Rare Disease we reach millions of patients each year. As a member of the Amgen team, youll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.

Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, youll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

Be part of Amgen's newest and most advanced drug substance manufacturing plant. When completed, the Amgen FleX batch facility will combine the latest in disposable technologies with traditional stainless steel equipment to allow for maximum flexibility in operations The FleX Batch facility will not only feature the best in-class drug substance manufacturing technologies with embedded industry 4.0 capabilities, but it will also integrate sustainability innovations to reduce carbon and waste, as part of Amgen's plan to be a carbon-neutral company by 2027.

**PrincipalProcess Engineer- Upstream/Downstream**

**What you will do**

In this vital role you will be joining the Facilities & Engineering (F&E) group to partner closely with the corporate engineering team to design, build, commission, and qualify new equipment and systems needed for drug substance production.You will lead technical projects, and drive innovation in product design and manufacturing processes. You will solve complex engineering problems, optimize processes, and ensure the company's engineering efforts align with strategic objectives. You will also provide leadership and guidance to the engineering team supporting 24/7 manufacturing and facility operations.

- **Site design, construction, start-up, and operational readiness:**

- Support the design and buildof manufacturing equipment systems by aligning design review processes and documents with site requirements, including equipment design and sizing, architecture and electrical distribution, and piping and instrumentation diagrams.

- Support factory acceptance testing working in partnership with global engineering during site installation, including reviewing protocols and resolving punch list items.

- Work with capital project team to ensure systems are installed and operatingsafely and comply with pertinent environmental health/safety practice, rules and regulations as well as Amgen global engineering requirements.Ensure that systems are installed per the design requirements.

- Execute and guide the commissioning and validation of systems to ensure their operational capability is aligned with manufacturing requirements and GMP regulation and on-time project delivery. Support execution of engineering and performance qualification runs while providing hypercare support as needed.

- Perform engineering assessments for plant equipment operations,implementing equipment modifications, and supporting engineering runs in support of new product/technology introductions as required.

- **Site Operations:**

- Provide system ownership for Upstream and/orDownstream Drug substance process equipment, areas, and systems providing end-to-end support for operations.

- Serve as a main point of contact for Process and equipment engineering function.

- Effectively collaborate with key customers and support groups(e.g. Manufacturing, Quality, Process Development, Maintenance, network partners) to ensure reliable plant operations.

- Work with original equipment manufacturers for breakdown and planned maintenance of process equipment as applicable.

- Leadidentifying and implementing engineering-based improvements or upgrades to processequipment systems.This may include developing business cases for improvements, identifying design requirements, and translating these requirements into process equipment/system design, specifications, and supporting the construction, startup, and validation of equipment.

- Develop master maintenance programs for equipment, ensure the availability of spare parts, andcoordinate maintenance activities to ensure systems are in proper working order.

- Ensure plant readiness and quality and regulatory compliance for internal audits, external agency audits, and partner audits for the process equipment.

- Providetechnical mastery andproblem-solvingleadership to proactivelyreduce production downtime. This includes leading technical root cause analysis and implementation of corrective/preventiveactions for families of systems.

- Lead new product/technology introductions by performing engineering assessments,equipment performance risk assessments, identifying gaps and owning their remediation, implementing equipment modifications, and supporting engineering runs.

- Provide mentorship and coaching to junior engineering peers when they encounter challenges and roadblocks, as appropriate.

- Demonstrate knowledge and understanding of how building and process automation systems interact with and impact process equipment and be able to effectively communicate automation issues and needs to support groups and to management.

- Effectively communicate the correct level of detail for process risks in a timely manner to support groups and leadership.

- Provide rotational on-call support and ensure 24x7 day-to-day reliability of Upstream and Downstream systemsfor plant operations.

- Up to 10% domestic/international travel.

**What we expect of you**

We are all different, yet we all use our unique contributions to serve patients. The engineering professional we seek enjoys challenges and is motivated to help serve patients with these qualifications.

**Basic Qualifications:**

- Doctorate degree and 2 years of engineering experience

OR

- Masters degree and 4 years of engineering experience

OR

- Bachelors degree and 6 years of engineering experience

OR

- Associates degree and 10 years of engineering experience

Or

- High school diploma / GED and 12 years of engineering experience

And

- 2 years of managerial experience directly managing people and/or leadership experience leading teams, projects, programs or directing the allocation of resources

**Preferred Qualifications:**

- Bachelors degree in Chemical or Mechanical Engineering or related technical field..

- 8+ years' of relevant work experience with 5+ years' experience in Biopharmaceuticaloperations/manufacturing environment focused on process and plant engineering function.

- Demonstrated people and/or project management and leadership experience.

- Direct knowledge of design and troubleshooting with GMP Biopharmaceutical Productionfacility equipment/systems with direct experience with Upstream and Downstream purification equipment such as cell culture reactors, centrifugation, chromatography, viral filtration skids, and UFDF skidsas well as other equipment needed to support these processes such as autoclaves, clean in place (CIP) systems, washers, clean steam, water for injection, etc.

- Experience with designing and operating equipment used in biopharmaceutical manufacturing.

- Experience with Tech Transfer, Process Design, and Commissioning & Qualification.

- Experience working in a regulated environment (e.g. cGMP, OSHA, EPA, etc.) andwith GMP quality systems/processes such as change control, non-conformances,corrective and preventative actions, and qualifications/validation

- Understanding of safety requirements working in a GMP Biopharmaceutical productionfacility.

- Independent, ambitious, organized, able to multi-task in project environments, and skilled incommunication, facilitation, and teamwork.

- Strong leadership, technical writing, and communication/presentation skills

- Work schedule flexibility as required to support 24/7 operations.

- Ability for domestic/international travel.

Senior Associate Manufacturing - Bulk Drug Substance Upstream - Days

**Join Amgens Mission of Serving Patients**

Youve worked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills, experience and passion to work toward your goals? At Amgen, our shared missionto serve patientsdrives all that we do. It is key to our becoming one of the worlds leading biotechnology companies, reaching over 10 million patients worldwide. Come do your best work alongside other innovative, driven professionals in this meaningful role.

Be part of Amgen's newest and most advanced drug substance manufacturing plant. When completed, the Amgen FleX Batch facility will combine the latest in disposable technologies with traditional stainless-steel equipment to allow for maximum flexibility in operations. The FleX Batch facility will not only feature the best in-class drug substance manufacturing technologies with embedded industry 4.0 capabilities, but it will also integrate sustainability innovations to reduce carbon and waste, as part of Amgen's plan to be a carbon-neutral company by 2027.

**Senior Associate Manufacturing - Bulk Drug Substance Upstream - Days**

**What you will do**

Lets do this! Lets change the world! In this dynamic role, you will be anSenior Associate in the manufacturing organization at Amgen North Carolina (ANC) supporting the facility expansion program and facility startup. Thisessentialrole will be part of a team responsible for manufacturingcell cultureoperationsincluding seed train, SUBs, Perfusion, RTF, Stainless Steel BRXs, Depth Filtration and Centrifugation,while partnering across functions to ensure successful operational readiness, technology transfer, and rampup of manufacturing operations within the new facility.

This role may require work outside standard business hours, including nonstandard shifts, as needed to support startup, commissioning and qualification (C&Q), and engineering execution.During this phase of thestartup, you will be expected toworkaMonday Friday schedule from 8am 5pm.As the business moves from C&Q to manufacturing operations, this essential positionwillwork ona 12-hour 2-2-3 schedule from 5:45 am to6:15pmsupporting our critical 24/7 manufacturing operations.As Amgen relies upon the regular attendance of all staff members to meet legitimate business needs, this role must be able to work assigned 12-hourshift, including during inclement weather, some holidays and requested overtime in support of our operations.

During early phases, this role will focus on operational readiness, training, and startup execution. As the facility transitions to steadystate operations, the role will shift toward routine manufacturing execution and continuous improvement.

**Compliance:**

- Completes work in accordance with established cGMP procedures and policies (Standard Operating Procedures \[SOPs\], Manufacturing Procedures \[MPs\], Job Hazard Analysis \[JHAs\], Code of Federal Regulations \[CFR\]) with strict adherence to safety and compliance

- Initiate Quality observations (Discrepancies, Deviations, Testing Results Analysis (TRA), etc.) as well as support or lead evaluations and investigations into quality observations

- Interact with regulatory agencies as needed and guided

- Assure proper gowning and aseptic techniques are always followed

**Operational Readiness & Facility Startup**

- Support operational readiness activities for facility expansion and startup

- Execute manufacturing readiness tasks including equipment preparation, procedure execution, and process walkthroughs

- Participate in commissioning, qualification, and startup activities as trained and assigned

- Provide operational feedback during startup activities to support safe, compliant, and efficient manufacturing

- Support readiness planning through execution of training, procedures, workflows, and operational practices required for startup and rampup

**Process/Equipment/Facilities:**

- Perform hands-on operations including set-up, cleaning, sanitization, monitoring of equipment of assigned area

- Run and monitor critical process tasks per assigned procedures

- Perform in-process sampling, operate analytical equipment, and complete process documentation (Electronic Batch Records \[EBR\])

- Complete washroom activities: cleaning equipment, small to large scale, used in production activities

- Identify, recommend, and implement innovative process improvements and optimizations related to daily routine functions

- Assist in the review of documentation for assigned functions (i.e., equipment logs, EBRs, ESPs)

- Collaborate cross-functionally (i.e., QA/QC, F&E (Facilities & Engineering), PPIC (Production Planning and Inventory Control), Mfg., PD (Process Development), Regulatory, etc.) in completing production activities

- Responsible for recognizing and elevating problems during daily operations

- Participate in the implementation of programs and CAPAs (Corrective Action Preventive Action) with an eye toward continuous improvement

- Drive safety in all operations, and assist the manager in escalating concerns as needed

- Maintain an organized, clean, and workable space

**Administrative:**

- Draft and revise documents (SOPs, technical reports, and MPs)

- Interacts with management as an advisor in planning and in escalating potential concerns with the schedule and/or process

**What we expect of you**

We are all different, yet we all use our unique contributions to serve patients. The hard-working professional we seek is a team player with these qualifications.

**Basic Qualifications:**

- High School Diploma/GED + 4 years manufacturing and/or other regulated environment experience OR

- Associates Degree + 2 years manufacturing and/or other regulated environment experience OR

- Bachelors Degree + 6 months manufacturing and/or other regulated environment experience OR

- Master's Degree

**Preferred Qualifications:**

- Completion of NC BioWork Certificate Program

- Experience in biotechnology or pharmaceutical plant start up

- Knowledge and process experience within a cGMP manufacturing facility or other highly regulated environment

- Basic understanding of Upstream operation (Vial Thaw, Inoculation/Cell Expansion, Single Use Bioreactor, Production Bioreactor, ATF, Harvest Centrifuge, Depth Filtration)

- Excellent verbal and written communication (technical) skills

- Proficient Microsoft Office skills, and knowledge of other electronic systems such as EBR/MES, Delta V, and Electronic Quality Systems

**What you can expect of us**

As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, well support your journey every step of the way.

In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards.

Senior Associate - Bulk Drug Substance Manufacturing Services - Days

**HOW MIGHT YOU DEFY IMAGINATION?**

At Amgen, if you feel like youre part of something bigger, its because you are. Our shared missionto serve patients living with serious illnessesdrives all that we do.

Since 1980, weve helped pioneer the world of biotech in our fight against the worlds toughest diseases. With our focus on four therapeutic areas Oncology, Inflammation, General Medicine, and Rare Disease we reach millions of patients each year. As a member of the Amgen team, youll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.

Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, youll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

Be part of Amgen's newest and most advanced drug substance manufacturing plant. When completed, the Amgen FleX Batch facility will combine the latest in disposable technologies with traditional stainless-steel equipment to allow for maximum flexibility in operations. The FleX Batch facility will not only feature the best in-class drug substance manufacturing technologies with embedded industry 4.0 capabilities, but it will also integrate sustainability innovations to reduce carbon and waste, as part of Amgen's plan to be a carbon-neutral company by 2027.

**Senior Associate - Bulk Drug Substance Manufacturing Services - Days**

**Live**

**What you will do**

Lets do this. Lets change the world! In this dynamic role, you will be a Senior Associate in the Manufacturing organization at Amgen North Carolina (ANC), supporting the ANC2 facility expansion and startup program. This essential role will be part of the Services team responsible for enabling manufacturing operations through weigh and dispense of raw materials, material receiving and handling, media, buffer, and solution preparation, and component preparation activities, including parts washing and autoclave operations.

As a Senior Associate, you will provide technical and operational support to the Services area, help coordinate daily activities, support training and qualification of staff, and promote safe, compliant, and reliable execution. You will partner across functions to support successful operational readiness, technology transfer, facility startup, and the ramp-up of manufacturing operations within the new facility.

This role may require work outside standard business hours, including non-standard shifts, as needed to support startup, commissioning and qualification (C&Q), and engineering execution. During this phase of startup, you will be expected to work a Monday through Friday schedule from 8:00 a.m. to 5:00 p.m. As the business transitions from C&Q to manufacturing operations, this essential position will move to a 12-hour, 2-2-3 schedule from 5:45 a.m. to 6:15 p.m., supporting critical 24/7 manufacturing operations.

Because Amgen relies on the regular attendance of all staff members to meet legitimate business needs, individuals in this role must be able to work their assigned 12-hour shift, including during inclement weather, on some holidays, and during requested overtime in support of operations.

During the early phases of the project, this role will focus on operational readiness, training, procedure development, equipment and process familiarization, startup execution, and coordination of Services activities. As the facility transitions to steady-state operations, the role will shift toward routine manufacturing execution, oversight of daily floor activities, troubleshooting, coaching and development of staff, cGMP documentation, and continuous improvement.

With general direction, the Senior Associate will support and help lead Services floor operations in accordance with current Good Manufacturing Practices (cGMP), applicable procedures, safety requirements, and established production schedules.

Responsibilities will include

Compliance:

- Completes work in accordance with established cGMP procedures and policies (Standard Operating Procedures \[SOPs\], Manufacturing Procedures \[MPs\], Job Hazard Analysis \[JHAs\], Code of Federal Regulations \[CFR\]) with strict adherence to safety and compliance

- Initiate deviation reports

- Interact with regulatory agencies as needed and guided

- Assure proper gowning and aseptic techniques are always followed

Process/Equipment/Facilities:

- Perform hands-on operations including set-up, cleaning, sanitization, monitoring of equipment and assigned area

- Run and monitor critical process tasks per assigned procedures

- Perform in-process sampling, operate analytical equipment, and complete process documentation (Electronic Batch Records \[EBR\])

- Complete washroom activities: cleaning equipment, small to large scale, used in production activities

- Identify, recommend, and implement innovative process improvements and optimizations related to daily routine functions

- Assist in the review of documentation for assigned functions (i.e., equipment logs, EBRs)

- Collaborate as part of a cross-functional team (i.e., QA/QC, F&E (Facilities & Engineering), PPIC, Mfg., PD (Process Development), Regulatory, etc.) in completing production activities

- Responsible for recognizing and elevating problems during daily operations

- Participate in the implementation of programs and CAPAs (Corrective Action Preventive Action) with an eye toward continuous improvement

- Drive safety in all operations, and assist the manager in escalating concerns as needed

- Maintain an organized, clean, and workable space

Administrative:

- Draft and revise documents (SOPs, technical reports, and MPs)

- Interacts with management as an advisor in planning and in escalating potential concerns with the schedule and/or process

**Win**

**What we expect of you**

We are all different, yet we all use our unique contributions to serve patients. The hard-working professional we seek is a team player with these qualifications.

**Basic Qualifications:**

- High School Diploma/GED + 4 years manufacturing and/or other regulated environment experience

Or

- Associates Degree + 2 years manufacturing and/or other regulated environment experience

Or

- Bachelors Degree + 6 months manufacturing and/or other regulated environment experience

Or

- Master'sDegree

**Preferred Qualifications:**

- Completion of NC BioWorks Certification Program

- Experience in biotechnology or pharmaceutical plant start up

- Knowledge and process experience within a cGMP manufacturing facility or other highly regulated environment

- Strong understanding of solution preparation, equipment preparation, and inventory control operations

- Excellent verbal and written communication (technical) skills

- Proficient Microsoft Office skills, and knowledge of other electronic systems such as EBR/MES, Delta V, and Electronic Quality Systems

**Thrive**

**What you can expect of us**

As we work to develop treatments that take care of others, we also work to care for our teammates professional and personal growth and well-being.

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.

Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including:

- Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.

- A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan

- Stock-based long-term incentives

- Award-winning time-off plans and bi-annual company-wide shutdowns

- Flexible work models, including remote work arrangements, where possible

**Apply now**

**for a career that defies imagination**

Objects in your future are closer than they appear. Join us.

**careers.amgen.com**

**#AmgenNorthCarolina**

Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Senior Associate Manufacturing - Bulk Drug Substance Downstream - Days

**Join Amgens Mission of Serving Patients**

Youve worked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills, experience and passion to work toward your goals? At Amgen, our shared missionto serve patientsdrives all that we do. It is key to our becoming one of the worlds leading biotechnology companies, reaching over 10 million patients worldwide. Come do your best work alongside other innovative, driven professionals in this meaningful role.

Be part of Amgen's newest and most advanced drug substance manufacturing plant. When completed, the Amgen FleX Batch facility will combine the latest in disposable technologies with traditional stainless-steel equipment to allow for maximum flexibility in operations. The FleX Batch facility will not only feature the best in-class drug substance manufacturing technologies with embedded industry 4.0 capabilities, but it will also integrate sustainability innovations to reduce carbon and waste, as part of Amgen's plan to be a carbon-neutral company by 2027.

**Senior Associate Manufacturing - Bulk Drug Substance Downstream - Days**

**Live**

**What you will do**

Lets do this! Lets change the world! In this dynamic role, you will be an Senior Associate in the manufacturing organization at Amgen North Carolina (ANC) supporting the facility expansion program and facility startup. Thisessentialrole will be part of a team responsible for manufacturingdownstream purification operations including column packing,columnchromatography, TFF,viralfiltration,viralinactivation, conjugation, and final fill,while partnering across functions to ensure successful operational readiness, technology transfer, and rampup of manufacturing operations within the new facility.

This role may require work outside standard business hours, including nonstandard shifts, as needed to support startup, commissioning and qualification (C&Q), and engineering execution.During this phase of thestartup, you will be expected toworkaMonday Friday schedule from 8am 5pm.As the business moves from C&Q to manufacturing operations, this essential positionwillwork ona 12-hour 2-2-3 schedule from 5:45 am to6:15pmsupporting our critical 24/7 manufacturing operations.As Amgen relies upon the regular attendance of all staff members to meet legitimate business needs, this role must be able to work assigned 12-hourshift, including during inclement weather, some holidays and requested overtime in support of our operations.

During early phases, this role will focus on operational readiness, training, and startup execution. As the facility transitions to steadystate operations, the role will shift toward routine manufacturing execution and continuous improvement.

**Compliance:**

- Completes work in accordance with established cGMP procedures and policies (Standard Operating Procedures \[SOPs\], Manufacturing Procedures \[MPs\], Job Hazard Analysis \[JHAs\], Code of Federal Regulations \[CFR\]) with strict adherence to safety and compliance

- Initiate Quality observations (Discrepancies, Deviations, Testing Results Analysis (TRA), etc.) as well as support or lead evaluations and investigations into quality observations

- Interact with regulatory agencies as needed and guided

- Assure proper gowning and aseptic techniques are always followed

**Operational Readiness & Facility Startup**

- Support operational readiness activities for facility expansion and startup

- Execute manufacturing readiness tasks including equipment preparation, procedure execution, and process walkthroughs

- Participate in commissioning, qualification, and startup activities as trained and assigned

- Provide operational feedback during startup activities to support safe, compliant, and efficient manufacturing

- Support readiness planning through execution of training, procedures, workflows, and operational practices required for startup and rampup

**Process/Equipment/Facilities:**

- Perform hands-on operations including set-up, cleaning, sanitization, monitoring of equipment of assigned area

- Run and monitor critical process tasks per assigned procedures

- Perform in-process sampling, operate analytical equipment, and complete process documentation (Electronic Batch Records \[EBR\])

- Complete washroom activities: cleaning equipment, small to large scale, used in production activities

- Identify, recommend, and implement innovative process improvements and optimizations related to daily routine functions

- Assist in the review of documentation for assigned functions (i.e., equipment logs, EBRs, ESPs)

- Collaborate cross-functionally (i.e., QA/QC, F&E (Facilities & Engineering), PPIC (Production Planning and Inventory Control), Mfg., PD (Process Development), Regulatory, etc.) in completing production activities

- Responsible for recognizing and elevating problems during daily operations

- Participate in the implementation of programs and CAPAs (Corrective Action Preventive Action) with an eye toward continuous improvement

- Drive safety in all operations, and assist the manager in escalating concerns as needed

- Maintain an organized, clean, and workable space

**Administrative:**

- Draft and revise documents (SOPs, technical reports, and MPs)

- Interacts with management as an advisor in planning and in escalating potential concerns with the schedule and/or process

**Win**

**What we expect of you**

We are all different, yet we all use our unique contributions to serve patients. The hard-working professional we seekis a team player with these qualifications.

**Basic Qualifications:**

- High School Diploma/GED + 4 years manufacturing and/or other regulated environment experience OR

- Associates Degree + 2 years manufacturing and/or other regulated environment experience OR

- Bachelors Degree + 6 months manufacturing and/or other regulated environment experience OR

- Master's Degree

**Preferred Qualifications:**

- Completion of NC BioWorks Certification Program

- Experience in biotechnology or pharmaceutical plant start up

- Knowledge and process experience within a cGMP manufacturing facility or other highly regulated environment

- Understanding of downstream purification operation (Column Chromatography, TFF, Viral Filtration, Viral Inactivation)

- Excellent verbal and written communication (technical) skills

- Proficient Microsoft Office skills, and knowledge of other electronic systems such as EBR/MES, Delta V, and Electronic Quality Systems

**Thrive**

**What you can expect of us**

As we work to develop treatments that take care of others, we also work to care for our teammates professional and personal growth and well-being.

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.

Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including:

- Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.

- A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan

- Stock-based long-term incentives

- Award-winning time-off plans and bi-annual company-wide shutdowns

- Flexible work models, including remote work arrangements, where possible

**Apply now**

**for a career that defies imagination**

Objects in your future are closer than they appear. Join us.

**careers.amgen.com**

**#AmgenNorthCarolina**

Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

R&D Operations Senior Manager

**Join Amgens Mission of Serving Patients**

At Amgen, if you feel like youre part of something bigger, its because you are. Our shared missionto serve patients living with serious illnessesdrives all that we do.

Since 1980, weve helped pioneer the world of biotech in our fight against the worlds toughest diseases. With our focus on four therapeutic areas Oncology, Inflammation, General Medicine, and Rare Disease we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, youll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.

Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, youll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

**Senior Manager, R&D Business Operations, Budget Management & Execution**

**What You Will Do**

Lets do this. Lets change the world. In this vital role, the Senior Manager, R&D Business Operations, Budget Management & Execution will lead the end-to-end budget execution process for assigned R&D organizations and serve as a trusted partner to functional leadership and R&D Finance.

The Senior Manager is accountable for the timely and high-quality delivery of annual budget planning, quarterly forecast updates and close activities, leadership reporting, and forward-looking financial insights. This role translates business priorities and changes in functional strategy into accurate budget projections and financial forecasts, helping leaders understand spending trends, risks, opportunities, and potential trade-offs.

The Senior Manager will also manage and develop members of the Budget Management & Execution team, establish consistent ways of working within the supported organization, contribute to capability standards and process improvements, and independently determine the operational approach required to meet financial and business objectives.

**Key Responsibilities**

- Lead the end-to-end budget management and execution process for assigned R&D organization(s), including annual budget planning, quarterly forecast updates, close activities, leadership updates, and other periodic financial deliverables.
- Serve as the primary Budget Management & Execution partner for functional leadership and R&D Finance, ensuring financial forecasts reflect business priorities, evolving strategy, and the prioritization of activities.
- Translate changes in baseline spend, portfolio or operational assumptions, resource needs, and business priorities into clear financial implications, forecasts, risks, and recommended actions.
- Maintain disciplined governance of budget plans, including reconciliation of actuals and commitments to plan and identification of meaningful forecast variances and emerging spending trends.
- Lead the collection, challenge, validation, and synthesis of planning assumptions and long-range spend drivers supporting annual budget and long-range planning activities.
- Develop leadership-ready financial reporting, analyses, and narratives that clearly communicate budget status, drivers of change, risks and opportunities, resource utilization, and decision points.
- Provide analytical support for functional initiatives, productivity opportunities, scenario development, and business case generation, including measurement of expected and realized benefits where appropriate.
- Enable execution of capital and operating expense plans through forecasting, funding alignment, financial tracking, and partnership with relevant functional and finance stakeholders.
- Provide expert budget execution support across the procure-to-pay process, resolving escalated issues and partnering with transactional finance, sourcing, and other business partners to improve execution and controls.
- Lead and coordinate finance-driven periodic activities such as accruals, purchase order maintenance, forecast updates, and ad hoc financial exercises.
- Serve as an advanced user of financial planning, reporting, and collaboration systems and promote consistent application of tools, processes, and data standards across the supported organization.
- Advance self-service and data-driven decision making by improving dashboards, reporting products, analytics, and other tools that provide leaders with timely and actionable financial insights.
- Contribute to the development and continuous improvement of Budget Management & Execution processes, standards, tools, and operating practices, identifying opportunities to simplify work, strengthen controls, improve cycle time, and increase scalability.
- Contribute business-partner perspective to R&D Finance, Corporate Finance, and other cross-functional initiatives affecting budget management and execution.
- Build and maintain strong partnerships across R&D functions, R&D Finance and FP&A, Global Strategic Sourcing, transactional finance, Supplier Management & Performance Analytics, and other business and corporate partners.

**People Leadership**

- Manage the day-to-day activities and priorities of assigned Budget Management & Execution team members, ensuring high-quality and consistent delivery across supported functions.
- Translate business plans and objectives into clear priorities, assignments, timelines, and expectations for the team.
- Provide coaching, feedback, training, and development to direct reports and other team members, helping build financial, analytical, business-partnering, and leadership capabilities.
- Allocate resources and adjust team priorities as business needs evolve while maintaining delivery of core financial commitments.
- Foster a collaborative, inclusive, customer-focused environment that encourages continuous improvement, strong judgment, and accountability for results.

**What We Expect of You**

We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a future-ready leader who brings financial and business acumen, operational rigor, strong people leadership, and a continuous-improvement mindsetsomeone who can simplify complexity, elevate insights, and influence across a matrix to drive outcomes.

**Basic Qualifications**

Doctorate degree and 2 years of biotech/pharma business operations and/or financial analytics experience

**OR**

Masters degree and 4 years of biotech/pharma business operations and/or financial analytics experience

**OR**

Bachelors degree and 6 years of biotech/pharma business operations and/or financial analytics experience

**OR**

Associates degree and 10 years of biotech/pharma business operations and/or financial analytics experience

**OR**

High school diploma / GED and 12 years of biotech/pharma business operations and/or financial analytics experience

**Preferred Qualifications**

- Advanced degree in business, finance, life sciences, or a related field.
- Demonstrated experience in budget management, financial planning, forecasting, reporting, and variance/root-cause analysis.
- Experience leading professional employees and/or demonstrated leadership of teams, projects, programs, or financial resources.
- Strong project and operational management experience, including the ability to establish priorities, manage competing deliverables, and drive high-quality execution.
- Working knowledge of the drug development process and how R&D organizations translate scientific and business strategy into portfolios, operating plans, and investment decisions.
- Demonstrated ability to partner effectively with functional leaders and finance stakeholders and translate business priorities into financial forecasts and actionable insights.
- Experience developing executive- or leadership-level financial narratives, presentations, analyses, and decision-support materials.
- Ability to work with detailed and complex information while identifying trends, implications, risks, and actions.
- Demonstrated proficiency with data visualization and collaboration tools such as Tableau, Smartsheet, and Microsoft Teams.
- Advanced Excel skills and strong command of the Microsoft Office suite.
- Experience with enterprise financial planning and procurement platforms such as SAP, Ariba, and Anaplan.
- Demonstrated ability to leverage automation, digital tools, and AI-enabled solutions to streamline workflows, improve controls, and elevate financial insights.
- Experience driving continuous improvement and change within business processes, tools, or operating models.
- Ability to thrive in a complex, matrixed environment; collaborate across organizational levels; influence without direct authority; and exercise sound judgment across multiple priorities.
- Exceptional written and verbal communication skills, including the ability to distill nuanced financial and business information into clear, concise, decision-ready messages.
- Strong relationship-building skills and a customer-service orientation, with a bias toward collaborative problem solving and solution delivery.
- Curious, proactive leader who learns quickly, takes initiative, develops others, and continuously raises the quality of team execution.

**What you can expect of us**

As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, well support your journey every step of the way.

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.

In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:

- A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
- A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
- Stock-based long-term incentives
- Award-winning time-off plans
- Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.

**Apply now and make a lasting impact with the Amgen team.**

**careers.amgen.com**

In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.

**Application deadline**

**External/Internal postings:**

Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.

**Internal only posting (or Pre-ID candidate):**

Amgen anticipates accepting applications until 1 week before the posting; however, we may continue accepting applications beyond this date if we do not receive a sufficient number of candidates.

**Sponsorship**

Sponsorship for this role is not guaranteed.

As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.

Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.