Manufacturing & Production

Amgen

Director, Bioprocess / Process Development Pivotal Drug Substance

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, Bioprocess / Process Development Pivotal Drug Substance**

**What you will do**

In this leadership role, you will be responsible for the development, characterization, scaleup, and support of drug substance cell culture and purification processes to enable commercial advancement of programs from Phase II/III through marketing applications. Located in Cambridge, MA and/or Thousand Oaks, CA, you will lead and develop a multisite organization of 30+ scientists and engineers while driving program success, safety culture, technical excellence, innovation, automation, and digital strategies.

You will support a diverse portfolio of biologics, including monoclonal antibodies (mAbs), BiTEs, bispecifics, biosimilars, and other novel proteinbased modalities, and play a key role in advancing latestage and commercial drug substance strategies across Amgens manufacturing network.

**Key Responsibilities**

- Lead a highimpact, multifunctional drug substance organization integrating cell culture and purification disciplines across multiple sites.
- Recruit, develop, and retain a strong and diverse team; manage portfolio prioritization and organizational resourcing.
- Advance integrated drug substance processes through commercial process development, process characterization, lifecycle management, and control strategy development.
- Partner with engineering, manufacturing, and external network collaborators to enable successful process transfer and commercialization.
- Author and review global regulatory filings (IND/INDa/MA) and respond to regulatory agency questions.
- Drive ideation, development, and deployment of innovative and differentiating bioprocess technologies.
- Contribute to Amgens scientific and regulatory eminence through publications, patents, and participation in external conferences and forums.
- Serve as a member of the Drug Substance Technology extended leadership team and contribute to business, organizational, and changemanagement strategies.

**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 and 4 years of scientific process development experience, OR
- Masters degree and 8 years of scientific process development experience, OR
- Bachelors degree and 10 years of scientific process development experience And

In addition to meeting at least one of the above requirements, you must have at least 4 years experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation or resources. Your managerial experience may run concurrently with the required technical experience referenced above

**Preferred Qualifications:**

- PhD in Biochemistry, Biochemical Engineering, Chemical Engineering, or related discipline
- 10+ years of experience in biopharmaceutical process development
- Minimum of 4 years of experience directly managing people
- Deep expertise in either cell culture bioreactor processes OR downstream purification processes
- Strong understanding of latestage biologics development including process design, characterization, validation (PPQ), and regulatory interactions
- Proven ability to provide scientific and engineering leadership on complex crossfunctional programs
- Demonstrated experience in statistical data analysis, technical decisionmaking, and seniorlevel communication
- Track record of developing talent through coaching, mentoring, and feedback
- Active engagement in the scientific community (publications, patents, industry forums)

**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.

Massachusetts

Manager, Environmental, Health, Safety and Sustainability

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.

**Environment, Health, Safety and Sustainability (EHSS) Manager**

**What you will do**

Lets do this! Lets change the world! Join our team as an Environmental, Health & Safety (EHS) Manager and help shape a world-class safety culture within a leading biotechnology organization. In this highly visible role, you will partner across the Manufacturing and Clinical Supply organization with specific focus on Quality Assurance, Quality Control, Manufacturing, Engineering, Facilities, and Warehouse Operations to drive strategic EHS initiatives that protect our people, support innovation, and enable operational excellence.

As a trusted advisor and leader, you will champion risk management, regulatory compliance, and continuous improvement while influencing business decisions across the organization. You'll have the opportunity to make a measurable impact by advancing safety performance, strengthening environmental stewardship, and fostering a culture where every employee is empowered to work safely.

Based at our headquarters in Thousand Oaks, California, this role offers the opportunity to collaborate with cross-functional teams, solve complex challenges, and help deliver life-changing therapies in a fast-paced, mission-driven environment.

**Primary responsibilities include:**

- Partner with Quality Assurance, Quality Control, Manufacturing, Facilities & Engineering, and Warehouse Operations to strengthen a proactive safety culture and effectively manage EHS risks across the organization.
- Serve as the subject matter expert and primary point of contact for critical EHS programs, including hazardous gas safety, lockout/tagout (LOTO), confined space entry, fall protection, non-routine and hazardous work, environmental compliance, and other core EHS programs.
- Lead ergonomic assessments and implement practical solutions that improve employee well-being and reduce musculoskeletal injury risks in both office and manufacturing environments.
- Develop and implement comprehensive EHS risk assessments that identify hazards, evaluate operational risks, and establish sustainable engineering, administrative, and procedural controls.
- Leverage EHS performance data and leading indicators to identify trends, drive continuous improvement initiatives, and measure progress against organizational objectives.
- Conduct workplace inspections, compliance assessments, and field observations to identify opportunities, reinforce safe behaviors, and ensure adherence to regulatory and company standards.
- Partner with cross-functional teams to integrate EHS requirements into change management activities, ensuring operational changes are evaluated for potential safety and environmental impacts before implementation.
- Lead incident response, investigations, and root cause analyses, driving effective corrective and preventive actions (CAPAs) that strengthen organizational learning and prevent recurrence.
- Facilitate EHS business reviews with functional leaders, providing strategic insights, monitoring performance, and driving accountability for key safety and environmental initiatives.
- Build trusted partnerships across all levels of the organization by providing expert EHS guidance, influencing decision-making, and promoting employee engagement through coaching, communication, and education.
- Support regulatory inspections, internal audits, and customer assessments while ensuring timely completion of corrective actions and sustained compliance.
- Champion continuous improvement by identifying innovative solutions that enhance operational efficiency, reduce risk, and advance the organization's EHS performance.

**What we expect of you**

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

**Basic Qualifications:**

- Doctorate degree *OR*
- Masters degree and 2 years of EHSS experience within a cGMP manufacturing environment *OR*
- Bachelors degree and 4 years of EHSS experience within a cGMP manufacturing environment *OR*
- Associates degree and 8 years of EHSS experience within a cGMP manufacturing environment OR
- High school diploma / GED and 10 years of EHSS experience within a cGMP manufacturing environment

**Preferred Qualifications:**

- Degree in safety, industrial hygiene, chemical engineering, mechanical engineering, chemistry, biology or other life science areas
- Demonstrated expertise in interpreting and applying Cal/OSHA regulations and other relevant EHS standards to ensure compliance within business operations and support risk-based decision-making.
- Proven ability to manage multiple projects and initiatives simultaneously while maintaining a high level of organization and quality.
- Demonstrated leadership in EHS programs within manufacturing or laboratory settings, with the ability to effectively influence both staff and management.
- 57 years of EHS experience in the pharmaceutical, biotechnology, or related life sciences industry, with a focus on implementing/managing EHS programs.
- Professional certification such as Certified Industrial Hygienist (CIH) and/or Certified Safety Professional (CSP) strongly preferred.
- Excellent communication and presentation skills, with a proactive, self-motivated approach to program development and project execution.
- Strong technical writing skills, with the ability to develop clear, concise, and compliant EHS documentation.
- Proficiency in Microsoft Office Suite and other relevant software tools used for data analysis, reporting, and presentations.

**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.

California

Counsel -- Global Commercial 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. 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.

**Counsel - Global Commercial Operations**

**What you will do**

Lets do this. Lets change the world. In this vital role you will be responsible for counseling Amgens Global Commercial Operations clients on a wide variety of legal and regulatory issues concerning promotion, sales, patient support programs, contracting, education and scientific exchange regarding biopharmaceutical products that are subject to oversight and regulation by several entities of the U.S. Federal government.

The primary responsibilities of this Counsel position will include:

- Advising and counseling on fraud and abuse matters relating to commercial activities involving members of the healthcare community (including payers, pharmacies, providers and patient and professional advocacy groups and associations), with emphasis on Federal Anti-Kickback Statute and False Claims Act
- Assessing proposed and ongoing patient support programs for legal risk
- Analyzing, reviewing and approving promotional, educational and patient support programs and materials
- Advising key stakeholders on legal, regulatory and policy developments to ensure that legal support is adapted to a rapidly changing environment
- Providing guidance on proposed sales and marketing strategies
- Advising on interconnected issues of law and policy relating to government health care programs
- Coordinating legal support by contributing as a member of cross-functional team and interacting with business and law department colleagues on various matters

**What we expect of you**

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

**Basic Qualifications:**

- J.D. degree or LL.M. degree from an accredited law school, admission to practice law in a U.S. jurisdiction

and

- two (2) years of experience practicing law

**Preferred Qualifications:**

- 4+ years of corporate, government and/or law firm experience.

- Proven superior legal skills, including excellent oral and written communication, legal analysis, drafting and negotiation skills
- Ability to lead and influence others
- Strong client service, business counseling, and a problem-solving focus
- Ability to manage multi-dimensional projects in a fast-paced environment
- Superior academic achievement
- Experience with health care law (Anti-Kickback Statute, False Claims Act, Food, Drug & Cosmetic Act, Medicare/Medicaid/340B) is a plus.

**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.

Supplier Governance 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.

**Supplier Governance Senior Manager**

**What you will do**

Lets do this. Lets change the world. In this vital role you will support Amgen sponsored clinical trials with a focus on key programs within Global Development Operations. You will be responsible for overseeing the performance and quality of Clinical Pharmacology CROs and laboratory suppliers and ensure alignment with Amgen's strategy and standards. You will develop strategic relationships and facilitating effective communication and collaboration among internal and external stakeholders. You will also contribute to process improvement initiatives, supplier evaluation and selection, and cross-functional projects.

- Facilitate and implement supplier governance meetings and operating reviews, monitor key performance indicators and perform issue management
- Support business functions with evaluation, selection, and startup of suppliers
- Collaborate with business leadership to identify business needs and priorities, and align supplier strategy and capabilities accordingly
- Build and maintain relationships with key internal and external partners, including study teams, functional leads, procurement, quality, compliance, and suppliers
- Lead proactive supplier risk management at portfolio and study level.
- Work with suppliers and Amgen stakeholders to identify process improvements and coordinate their development and implementation, ensuring adherence to best practices and compliance requirements
- Assist with standardizing and aligning clinical trial execution across programs and portfolio
- Support the assessment and implementation of technologies and innovations
- Lead and contribute to cross-functional initiatives and special projects
- Facilitate mentoring, training, and career development of direct reports, and manage their performance and feedback

**What we expect of you**

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

**Basic Qualifications:**

- Doctorate degree and 2 years of Clinical experience

**Or**

- Masters degree and 4 years of Clinical experience

**Or**

- Bachelor's degree and 6 years of Clinical experience

**Or**

- Associate's degree and 10 years of Clinical experience

**Or**

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

**Preferred Qualifications:**

- BS/BA/BSc in the sciences or RN
- 9 years work experience in life sciences or medically related field, including 6 years of biopharmaceutical clinical research experience (clinical research experience obtained working on clinical trials at a biotech, pharmaceutical or CRO company)
- Experience with Clinical Pharmacology
- Experience working in a laboratory
- Experience working with and/or oversight of suppliers working on clinical trials
- Experience with risk management
- Experience leading direct reports
- Experience working in a global, matrix organization
- Knowledge of Good Clinical Practices (GCP), FDA regulations and guidelines, and international regulatory requirements/guidelines
- Clinical trials execution experience
- Project management experience
- Proficiency in proactive issue management
- Experience writing and presenting clearly to Senior Management
- Demonstrated ability to communicate effectively with a diverse audience
- Excellent interpersonal, organizational, supervisory skills
- Professional collaboration and leadership skills

**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.

District of Columbia

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**

**What you will do**

Lets do this. Lets change the world. In this vital role, as a member of the Amgen Manufacturing & Clinical Supplies (MCS) Facilities & Engineering (F&E) Automation team, you will lead technical projects supporting Clinical & Commercial Plant Automation programs and Capital projects, including complex and challenging automation initiatives that require proven understanding of various automation platforms, integration between different platforms, analytical problem-solving techniques, critical thinking, project management, product lifecycle management and Operational Excellence. You will require extensive understanding and background in process control & automation systems, capital construction projects, engineering projects lifecycle phases, and lifecycle management of process automation systems and technologies for Amgen.

**Responsibilities include:**

- Lead technical projects as automation technical lead on complex capital construction projects including lifecycle asset management projects.
- Collaborate with the site process engineering team to understand key process requirements, develop and maintain process control/automation solutions using DeltaV Distributed Control System (DCS), Rockwell Programmable Logic Controllers (PLC), Human Machine Interfaces (HMI) and Supervisory Control and Data Acquisition systems (SCADA) on Virtual Server infrastructure.
- Support functional area projects focused on improving process equipment/utilities/facilities -to- sophisticated unit operation skids to integrate new drug substance & drug product manufacturing technologies into clinical/commercial facility.
- Lead/support technical root cause analysis, incident investigations, and troubleshooting on process control issues related to plant operations.
- Partner closely with the Capital project team to design, build, commission, and qualify new equipment and systems needed for MCS operations.
- Support Commissioning & Qualification efforts including Automation Installation Verification/Automation Checkout/Functional Testing.
- Partner with various organizational units to support tasks including operational readiness, document reviews, deviation investigation and change controls
- Develop and maintain detailed specifications, Standard Operating Procedures, and Operating standards that impact multiple organizational units
- Develop domain expertise to support operations upon startup, focusing on manufacturing process automation
- Provide leadership and guidance to the Automation Engineering team supporting 24 x 7 and troubleshooting to Manufacturing & facility Operations
- 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
- Collaborate with Amgen Pilot Plants, Drug Substance & Drug Product Plant network to improve the automation design for Manufacturing & Pilot Plant Operations.
- Provide support to the capital project team with a strong focus on safety and on-time facility startup
- Provide mentoring to develop and accelerate site technical automation team capabilities.

**What we expect of you**

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

**Basic Qualifications:**

- Doctorate degree OR
- Masters degree and 2 years of Manufacturing Automation Systems Engineering experience OR
- Bachelors degree and 4 years of Manufacturing Automation Systems Engineering experience OR
- Associates degree and 8 years of Manufacturing Automation Systems Engineering experience OR
- High school diploma / GED and 10 years of Manufacturing Automation Systems Engineering experience

**Preferred Qualifications:**

- Degree in Electrical Engineering 10or Computer Science, Chemical Engineering or Biotech Engineering
- Extensive experience with understanding and background in Emerson DeltaV Systems, Rockwell Automation SCADA & PLCs, PI, Virtual Server infrastructure - Design, Engineering, Configuration, Programming, Testing, Installation, Commissioning and lifecycle management of automation, and field instrumentation
- Direct knowledge of Automation design, experience in process control engineering and troubleshooting with GMP biopharmaceutical production facility equipment/systems such as media, harvest, bioreactors, chromatography, vial filtration, and ultrafiltration/diafiltration, and integrating various OEM automation software.
- Demonstrated experience with continuous improvements resulting in enhanced safety, system reliability, and efficiency (e.g. cycle times, and reduced plant utilities usage etc.) related to Drug Substance & Drug Product Plant Operations.
- Demonstrated hands-on experience in developing process control strategies for New Products
- Familiarity with Upstream and Downstream unit operations.
- Experience in Capital Project Lifecycle Management: Conceptual Design, Scope and cost estimate development, business case development, detailed design, engineering and validation documentation and project execution.
- The ideal individual must be a self-directed standout colleague ready to mentor and develop engineering staff and adopt a team-based culture that relies on collaboration for effective
- 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.

**3+ 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 sophisticated troubleshooting activities with network & server infrastructure team.
- System Integration using OPC, Profibus, and DeviceNet technologies.
- Compliance and regulatory requirements such as 21 CFR Part 11, ASTM 2500, 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.

Director, Scientific and Operations Intelligence, Obesity

**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, Scientific and Operations Intelligence, Obesity**

This role owns the non-commercial Obesity Insights & Analytics agenda across scientific domains, including R&D, Medical, and Clinical Development, and operations domains, including Clinical Operations, Supply, and related Operations functions. As the trusted Insights & Analytics partner to senior leaders across these functions, the Director connects priorities, surfaces cross-functional dependencies, frames the questions with the greatest potential to improve decisions and outcomes, and mobilizes the right data and expertise to deliver clear recommendations for Obesity and Related Conditions leadership.

During the initial capability build, the Director will operate as an agile enterprise problem solver, flexing across the highest-priority functional and cross-functional needs. In parallel, the Director will build the long-term team, operating model, and recurring portfolio required to create sustained value.

The Director is accountable for prioritization, problem framing, analytical strategy and delivery, executive synthesis, and decision-impact measurement, partnering with the India-based Scientific and Operations Intelligence capability and other experts to scale delivery. Commercial Insights & Analytics and Competitive Intelligence are outside the remit. Success is measured by decisions improved, risks anticipated, and value created.

**Key Responsibilities**

- Build and sustain trusted relationships with senior leaders across R&D, Medical, Clinical Development, Clinical Operations, Supply, and related Operations functions to understand evolving priorities, connect interdependencies, and shape the Insights & Analytics agenda. Anchor each priority to a clear question, decision date, decision owner, and value at stake, and ensure insights translate into decisions and action.
- Serve as an agile problem-solving leader across the scientific and operations remit, rapidly deploying to the most consequential functional and cross-functional priorities rather than operating through fixed workstreams.
- Lead priority work end to end: define the decision and hypotheses; determine the analytical approach; mobilize the right data, capabilities, and experts; synthesize findings; recommend a course of action; and track impact.
- Integrate scientific and operational information into decision-ready views of options, dependencies, uncertainties, and trade-offs, including research prioritization, development choices, evidence generation, trial execution, supply capacity, and readiness.
- Build reusable decision products and analytical capabilities, including scenario models, evidence maps, risk dashboards, decision trees, and leading indicators. Apply advanced analytics and AI where they materially improve quality, speed, or scale.
- Build the long-term team and operating model, including intake and prioritization, stakeholder engagement, work-product standards, governance, and an effective delivery model across the India-based Scientific and Operations Intelligence capability, functional analytics teams, and subject-matter experts.
- Create a high-performing culture of intellectual honesty, constructive challenge, analytical rigor, and action, with strong standards for scientific integrity, compliance, privacy, data governance, and reproducibility.

**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 someone with these qualifications.

**Basic Qualifications**

- Doctorate degree and 4 years of relevant experience OR
- Masters degree and 7 years of relevant experience OR
- Bachelors degree and 9 years of relevant experience

**Preferred Qualifications**

- Advanced degree in life sciences, medicine, pharmacy, public health, epidemiology, data science, engineering, operations research, business, or a related field.
- Ten or more years of experience in biopharma, biotechnology, healthcare, or life sciences consulting, with deep expertise in at least one relevant scientific or operations domain, meaningful experience in another, and demonstrated ability to integrate across functions.
- Demonstrated success framing ambiguous, high-stakes questions and translating complex evidence into recommendations that changed or accelerated a senior leadership decision.
- Proven ability to deliver near-term impact while building a new capability, operating model, or team across a complex global organization.
- Strong understanding of drug discovery and development, medical evidence, clinical trial design and execution, and biopharmaceutical supply operations, with fluency in relevant data, scenario modeling, visualization, and responsible applications of AI.
- Experience in obesity, cardiometabolic disease, or another complex and rapidly evolving therapeutic area is strongly preferred.
- Exceptional executive communication, judgment, and ability to influence, challenge constructively, and create alignment in a global matrix.

**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.

\#obesity

Front Line Manufacturing Manager (Bulk Drug Substance - Downstream) - Night Shift

**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.The AmgenFleXBatch facilitycombinesthe latest in disposable technologies with traditional stainless-steel equipment to allow for maximum flexibility in operations. TheFleXBatch facility not only featuresthe best in-class drug substance manufacturing technologies with embedded industry 4.0 capabilities, but it also integratessustainability innovations to reduce carbon and waste, as part of Amgen's plan to be a carbon-neutral company by 2027.

**Manager Manufacturing(Downstream)- Night Shift**

**Live**

**What you will do**

Letsdo this.Letschange the world. Inthesevital anddynamicrolesyou will beanon-shift front line manager in manufacturing.Theworkingscheduleis based onaday or night shift (12-hour)rotation.

The essential position, which supports our critical 24/7 manufacturing operations, works a 12-hour 2-2-3 schedule from 5:45pm to 6:15am.

Asamanufacturingleaderyou will overseeteamsof manufacturing associateswith differing levels of experience who willberesponsible forthe manufacture of GMP drugsubstances.Through structured onthefloor presence, youwillchampion a safe and compliant production environment.Asan active participant and role model inaLean and continuous improvementculture,the manager willimbedtheseprinciplesonto the manufacturing floor.

Through your leadership, you willoverseeteams intechnical,on thefloor operations ina biotechnologyproduction operation.In addition, you will supportthe developmentof your staff throughcoaching, hiring, andmentorship.

Font-lineManagerwillassistin defining areaobjectives,identifyingimprovement opportunities, and leading change efforts; effectively directing their team anddeliveringshort-and long-termAmgen Operational goals.

Compliance:

- Ensure safe working environment

- Ensure Amgen policies are followed, including cGMP and CFR (Code of Federal Regulations) compliance of assigned areas

- Evaluatecurrent operating procedures and recommend changes to management tooptimizeproduction.

- Assure all corporate change control procedures are followed, and Regulatory and QA are notified prior to the changes

- Interact with regulatory agencies as needed

- Assure proper gowning and aseptic techniques are followed

Staff Supervision:

- Engagestaff and build relationships of trust and respect while driving team performance and continuous improvement

- Recruit, train, evaluate,coachanddevelopstaff

- Mentor and coach staff members to live by the Amgen Values

- Develop and implement trainings plans and programs, to ensure staff are prepared and compliant

- Ensure adherence to production schedule and maintenance activities

- Interacts with management inoptimizingorganizational structure and responsibilities

- Ensure plant safety through auditing,evaluations, and cross functional walks

- Ensure gowning and aseptic techniques training programs are maintained

Process/Equipment/Facilities:

- Demonstrate technical mastery of manufacturing processes

- Collaborate with cross-functional teams (i.e.,QA/QC, F&E, PPIC,Mfg, PD, Regulatory, etc.) in completing production activities

- Develop,implementand assessCAPAs andsolutionstocomplex problems

- Responsible forelevating andresolving problems duringdailyoperations

- Oversees set up, execution,and completion of critical manufacturing processes/tasks

Administrative:

- Interacts with management in planning,developingandmaintainingbudget

- Assistin developing andmaintainingdepartment goals

**Win**

**What we expect from you**

We are all different, yet we all use our unique contributions to serve patients. Thebiotechnologyprofessional weseekis amanagerwith these qualifications.

**Basic Qualifications**

- Doctoratedegree OR

- Masters degreeand3years ofManufacturing or Operationsexperience OR

- Bachelors degree and5years ofManufacturing or Operationsexperience OR

- Associates degree and 10 years of ManufacturingorOperations experience OR

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

- AND Previous managerial experience directly managing people and/or experience leading teams, projects, programs or directing the allocation of resources

**Preferred Qualifications**

- Bachelors degree in Life Sciences or Engineering

- Demonstrated strong leadership skills and technical understanding of biotechnology production operations

- Experience inbiotechnology or pharmaceutical plant start up

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

- Previousknowledge and experience within a cGMPenvironment

- 5+years process experience in a cGMP manufacturing facility

- 3+ years of experience in a production Area Lead, Specialist or Manager role

- Strong leadership and teambuilding skills (coaching, mentoring, counseling)

- Experience with performance management including performance reviews

- Conflict Resolution,analytical problem solving,and projectmanagement skills

- Thorough understanding of regulatory requirements

- Excellent verbal and written communication (technical) skills

- Excellent computer skills with Microsoft, EBR/MES, Delta V, 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 annual base salary range for this opportunity in the U.S. is provided below.

In addition to the base salary, Amgen offers a Total Rewards Plancomprisinghealth 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 nowfor a career that defies imagination**

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

**careers.amgen.com**

**#AmgenNorthCarolina**

North Carolina

Sr. Director Environment, Health and Safety

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 Director, Global Safety & Risk Programs**

**What you will do**

Lets do this. Lets change the world! The Senior Director, Global Safety & Risk Programs is a strategic enterprise leader responsible for defining and executing Amgen's global safety and operational risk strategy. This role leads the transformation, governance, and continuous evolution of enterprise safety programs to enable sustainable business growth, operational excellence, innovation, and organizational resilience.

Reporting to the Head of Global Environment, Health & Safety (EHS), this leader partners across Operations, Global Engineering, Research & Development, Product Stewardship, Corporate Functions, Security, and Digital Technology & Innovation to modernize safety management systems, accelerate digital transformation, and integrate risk management into business decision-making.

This role will champion innovation, leverage emerging technologies and AI-enabled insights, strengthen enterprise capabilities, and build an integrated safety culture that enables Amgen to deliver with greater speed, agility, and confidence.

**Key Responsibilities**

**Enterprise Strategy & Transformation**

- Develop and execute Amgen's enterprise Safety & Risk strategy aligned with corporate priorities and long-term business objectives.
- Lead the transformation and modernization of global safety programs to improve organizational effectiveness and operational performance.
- Establish a multi-year roadmap to evolve enterprise safety capabilities, governance, and risk management practices.
- Benchmark leading biotechnology, pharmaceutical, and high-reliability organizations to continuously improve enterprise capabilities.
- Foster a culture of innovation, agility, and continuous improvement across the global EHS organization.

**Innovation & Digital Enablement**

- Drive innovation by integrating AI, predictive analytics, automation, and digital technologies into enterprise safety programs.
- Develop advanced dashboards and leading indicators that enable proactive risk management and executive decision-making.
- Champion digital transformation initiatives that simplify processes, improve user experience, and increase organizational efficiency.
- Evaluate emerging technologies to strengthen workforce protection and operational resilience.

**Global Safety & Critical Risk Programs**

Provide enterprise leadership and governance for:

- Occupational Safety
- Critical Risk Management
- Serious Injury & Fatality (SIF) Prevention
- Contractor Safety Excellence
- Human & Organizational Performance (HOP)
- Control of Work
- Electrical Safety
- Machine Safety
- Confined Space
- Lockout/Tagout
- Working at Heights
- Ergonomics
- Powered Industrial Vehicles
- Line-of-Fire Prevention
- Learning Teams & Operational Learning

Ensure programs remain scalable, standardized, and adaptable to evolving business needs.

**Enterprise Risk Management**

- Advance enterprise risk management capabilities through data-driven decision-making and systems thinking.
- Establish governance for identifying, assessing, and mitigating operational risks across the enterprise.
- Integrate risk management into capital projects, engineering design, manufacturing operations, R&D, and business planning.
- Develop enterprise risk intelligence and predictive capabilities that improve organizational resilience.

**Operational Excellence & Organizational Effectiveness**

- Lead initiatives that simplify processes, eliminate unnecessary complexity, and improve execution across the enterprise.
- Drive integration between safety, engineering, quality, operations, and continuous improvement initiatives.
- Ensure safety programs enable productivity, innovation, and operational performance rather than acting as standalone compliance activities.
- Promote systems thinking and cross-functional collaboration to improve end-to-end business performance.

**Culture, Leadership & Change Management**

- Lead enterprise change management efforts that strengthen safety culture and organizational performance.
- Build leadership capability in Human & Organizational Performance (HOP), learning culture, and risk-based decision-making.
- Partner with senior leaders to embed safety into business transformation initiatives.
- Foster psychological safety, frontline engagement, accountability, and continuous learning.

**Governance, Assurance & Compliance**

- Establish enterprise governance frameworks that ensure consistency, transparency, and accountability.
- Monitor program effectiveness through KPIs, leading indicators, and executive dashboards.
- Lead enterprise audits, assessments, and management reviews.
- Ensure compliance while advancing innovative approaches that improve business value.

**Talent & Organizational Capability**

- Build and develop a high-performing global organization capable of supporting future business needs.
- Coach and mentor emerging leaders.
- Develop critical technical capabilities and succession plans.
- Foster an inclusive, collaborative, and innovation-driven culture.

**The successful leader will:**

- Lead the transformation of Amgen's global safety and risk programs to meet future business needs.
- Accelerate digital innovation and AI adoption across EHS.
- Improve enterprise risk visibility, predictive capabilities, and decision-making.
- Strengthen organizational resilience and critical risk management.
- Enable safer, faster, and more efficient business execution.
- Increase cross-functional integration and operational effectiveness.
- Build a high-performing organization that continuously innovates and adapts.
- Position Global EHS as a strategic business partner that enables growth, operational excellence, and long-term enterprise success.

**What we expect of you**

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

**Basic Qualifications:**

- Doctorate degree and 5 years of leading transformation safety and risk experience OR
- Masters degree and 9 years of leading transformation safety and risk experience OR
- Bachelors degree and 11 years of leading transformation safety and risk experience AND

In addition to meeting at least one of the above requirements, you must have at least 5 years experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation of resources. Your managerial experience may run concurrently with the required technical experience referenced above

**Preferred Qualifications:**

- Demonstrated success leading enterprise transformation initiatives within biotechnology, pharmaceutical manufacturing, engineering, or similarly regulated industries like oil and gas.
- Proven experience driving organizational transformation, innovation, and digital modernization.
- Strong system-thinking mindset with the ability to simplify complex global organizations.
- Experience leveraging AI, advanced analytics, and digital technologies to improve business performance.
- Expertise in enterprise risk management, organizational resilience, and operational excellence.
- Experience influencing executive leadership and leading change across complex matrix organizations.
- Strong business acumen with the ability to balance risk, innovation, and execution.
- Exceptional strategic thinking, executive communication, and stakeholder management skills.

**Critical Leadership Competencies**

- Strategic Leadership
- Enterprise Transformation
- Innovation & Digital Mindset
- Systems/Process Thinking
- Organizational Effectiveness
- Business Enablement
- Operational Excellence
- Executive Influence
- Change Leadership
- Risk Intelligence
- AI & Digital Adoption
- Continuous Improvement
- Organizational Resilience
- Cross-Functional Integration
- Data-Driven Decision Making
- Talent Development
- Collaboration & Influence
- Customer & Patient Focus

**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.

Process Development Sr Principal 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 Principal Scientist**

**What you will do**

In this vital role, you will lead a team of analytical scientists responsible for developing, transferring, validating, and implementing analytical methods to support late-phase oligonucleotide programs through commercialization. As the Attribute Sciences Team Lead (ASTL), you will provide scientific, technical, and strategic leadership, driving the development and application of analytical tools to characterize critical quality attributes and advance product and process understanding. You will leverage platform expertise and deep product attribute knowledge to shape analytical control strategies and enable successful process performance qualification (PPQ), regulatory submissions, marketing authorization, and commercial launch. In close collaboration with Process Development, Manufacturing, Quality, Regulatory, and external partners, you will influence cross-functional decisions, resolve complex technical challenges, and ensure successful execution of commercialization strategies.

- Lead and mentor a group of analysts in supporting process development. Provide career development guidance to the team members.
- Lead analytical method development for synthetic small molecules, synthetic peptide, and/or SiRNA manufacturing, release testing and characterization.
- Collaborate closely with drug substance and drug product process development colleagues to achieve project objectives.
- Define analytical control strategies and implement methodologies for development of late phase clinical programs.
- Provide concise summary to cross-functional leadership for endorsement of key decisions.
- Oversee activities at contract manufacturing and testing sites.
- Author technical reports and analytical Chemistry, Manufacturing and Controls (CMC) sections in regulatory documents. Address analytical and product quality inquiries from health authorities.

**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 PhD OR PharmD OR MD and 2 years of Scientific experience

OR

Masters degree and 5 years of Scientific experience

OR

Bachelors degree and 7 years of Scientific experience

**Preferred Qualifications:**

- PhD in Analytical Chemistry, Organic Chemistry, Physical Chemistry, Material Sciences, Pharmaceutical Sciences, or related discipline.
- Experience in the pharmaceutical or biotech industry, focusing on process and product development, and analytical method development for small molecule, peptide, and/or oligonucleotide drug substances and products.
- Strong understanding of small molecule analysis, structure elucidation and solid-state characterization informed by knowledge of organic chemistry.
- Strong understanding of peptide and/or oligonucleotide structural elucidation and characteristics that relate to quality of peptide and/or oligonucleotide.
- Hands on experience in method development, validation, and transfer for in-process, release, and stability testing
- Strong experience in oligonucleotide method development, characterization, and analytical control strategy especially having mass spectroscopy (MS) experience.
- 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 concise summary to 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.

Senior Manager: Manufacturing Material Handling

**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. The AmgenFleXBatch facility combines the latest in disposable technologies with traditional stainless-steel equipment to allow for maximum flexibility in operations. TheFleXBatch facility not only features the best in-class drug substance manufacturing technologies with embedded industry 4.0 capabilities, but it also integrates sustainability innovations to reduce carbon and waste, as part of Amgen's plan to be a carbon-neutral company by 2027.

**Senior Manager: Manufacturing Material Handling**

**Live**

**What you will do**

Let'sdo this.Let'schange the world. As a Senior Manager of Manufacturing Material Handling, you will provide leadership and guidance to the team responsible for 24/7 GMP material handling operations supporting manufacturing across the facility.

In this vital role as a member of the Manufacturing leadership team, the Senior Manager, Manufacturing Material Handling, will collaborate cross-functionally to enable the manufacture of drugsubstancein a newstate-of-the-artmanufacturing facility. This roleis responsible forleading and developing Material Handling Front-Line Managers who oversee teams supporting the receipt, staging, movement, storage, inventory control, and delivery of GMP materials between the warehouse and manufacturing operations. Additionally, you will be accountable for organizational design, hiring, development, and training complianceofthe Material Handling organization to ensure safe, reliable, and uninterrupted manufacturing operations. The position will also provide leadership and oversight for operational readiness activities to ensure successful facility start-up and sustained commercial manufacturing performance.

**Responsibilities:**

- Develop andretaina diverse, high-performing Material Handling organization in alignment with operational readiness schedules to support successful facility startup and commercial GMP operations.

- Foster a strong safety, quality, and compliance culture while championing continuous improvement across all Material Handling activities.

- Collaborate as one team with Manufacturing, Warehouse Operations, Quality, Engineering, Supply Chain, Process Development, Automation, and network partners to ensure reliable execution of manufacturing operations.

- Lead the execution and continuous improvement of end-to-end material flow processes, ensuring the right materials are available at the right location and time to support uninterrupted manufacturing.

- Oversee inventory accuracy, material reconciliation, cycle counting, and GMP inventory control processes while ensuring compliance with regulatory and internal quality requirements.

- Own the Manufacturing Material Transfer Equipment program, ensuring equipment lifecycle management, availability, qualification, maintenance coordination, and operational readiness.

- Partner with Supply Chain and Warehouse Operations tooptimizematerial staging, replenishment strategies, and production scheduling while minimizing operational risk.

- Provide leadership in troubleshooting operational issues affecting material availability andestablishrobust escalation and 24/7 support processes.

- Lead investigations related to material handling deviations, inventory discrepancies, and material management events while driving effective root cause analysis and corrective actions.

- Develop and implement departmental strategies aligned with organizationalobjectiveswhile driving Operational Excellence, Lean Manufacturing, and continuous improvement initiatives.

- Lead and support internal and regulatory inspections for areas of responsibility, includinginspectionreadiness, response development, and sustainable compliance strategies.

- Deliver against organizational financial commitments whileoptimizinglabor, inventoryutilization, and operational efficiency.

**Win**

**What we expect of you**

We are all different, yet we all use our unique contributions to serve patients. The experienced professional weseekis a collaborative partner with these qualifications.

**Basic Qualifications:**

Doctorate degree and 2 years of Manufacturing & Operations experience Or

Masters degree and 6 years of Manufacturing & Operations experience Or

Bachelors degree and 8 years of Manufacturing & Operations experience Or

Associate's degree and 10 years of Manufacturing & Operations experience Or

High School diploma/GED and 12 years of Manufacturing & Operations experience

AND2 years of managerial experience directly managing people and/or leadership experience leading teams, projects, programs or directing the allocation of resources

**Preferred Qualifications**

- Demonstrated managerial experience supporting GMP manufacturing operations in abiologicsor pharmaceutical manufacturing environment.

- Experience leading GMP material handling, manufacturinglogistics, inventory management, or warehouse operations supporting manufacturing.

- Demonstrated experience implementing Operational Excellence, Lean Manufacturing, and continuous improvement methodologies.

- Experience with electronic inventory management systems (SAP, MES, electronic batch records, barcode/RFID technologies, or equivalent).

- Working knowledge of GMP material management, inventory control, material traceability, and regulatory compliance requirements.

- Cross-functional experience partnering with Manufacturing, Supply Chain, Engineering, Quality, and Process Development organizations.

- Excellent communication, leadership, organizational, and problem-solving skills with the ability to influence across multiple organizations.

- Demonstrated ability to develop high-performing teams and foster an inclusive, accountable, and collaborative culture.

**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.

- Vast opportunities to learn and move up and across our global organization

- Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act

- Generous Total Rewards Plancomprisinghealth, finance and wealth, work/life balance, and career benefits

Apply now

for a career that defies imagination

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

**careers.amgen.com**

\#AmgenNorthCarolina

Associate Director- Supply Chain Data Science

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 Director of Data Science Global Supply Chain Digital**

**What you will do**

Lets do this. Lets change the world. The Global Supply Chain Digital Team at Amgen is seeking an Associate Director of Data Science to join the cross-functional Global Supply Chain organization, based either at our Thousand Oaks headquarters or remotely.

In this vital role, you will lead the development and deployment of advanced analytics, AI/ML, GenAI, and digital solutions that transform Global Supply Chain operations and enable reliable delivery of critical medicines to patients worldwide. This role combines strategic leadership with deep technical expertise. In addition to leading advanced data science initiatives, the Associate Director will help establish and scale Amgens India-based digital capability team supporting Global Supply Chain. This includes helping define the organizational structure, operating model, governance, and delivery processes for a team of data scientists and digital developers, while providing ongoing leadership and oversight once the organization is established. We are seeking a Data Science leader with expertise in AI/ML, advanced analytics, digital product development, and modern data architecture, along with a strong understanding of supply chain and manufacturing operations. The successful candidate will collaborate closely with Supply Chain, Operations, Finance, IT, and Digital Technology teams to develop scalable solutions that improve forecasting, planning, inventory optimization, productivity, and operational performance.

**Responsibilities may include, but are not limited to:**

- Design and deploy AI, GenAI, Agentic, and advanced analytics solutions to transform end-to-end Supply Chain operations.
- Lead the development of scalable digital products, analytical applications, and automation capabilities using large and complex datasets.
- Help establish and scale a Global Supply Chain Digital capability team in India, including organizational design, operating model development, governance, and delivery processes.
- Provide leadership and oversight for global teams of data scientists and digital developers across onshore and offshore locations.
- Partner with business leaders, IT, and data engineering teams to deliver robust, scalable, and business-aligned analytics solutions.
- Develop impactful visualizations and executive-level insights that support strategic decision-making and operational transformation.
- Explore and implement emerging technologies and modern data science practices to enhance organizational capabilities.
- Lead productivity analytics initiatives and develop KPIs and performance metrics that drive operational excellence across the global supply chain.
- Mentor and develop Digital/Data Science staff while fostering a culture of innovation, collaboration, and continuous improvement.

**Required Skills**

- People leadership and organizational management experience
- Experience building and scaling global or offshore technical teams
- Experience developing scalable data science applications for manufacturing or supply chain operations
- Strong expertise in AI/ML, GenAI, advanced analytics, and digital product development
- Proficiency in Python and SQL
- Experience working with large, complex datasets and modern data architecture
- Experience working in Agile teams to deliver digital products
- Experience with data visualization tools such as Spotfire and Matplotlib
- Strong communication, stakeholder management, and cross-functional collaboration skills

**What we expect of you**

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

**Basic Qualifications:**

- Doctorate degree and 3 years of Engineering, Computer Science, Operations, Analytics, Data Science, or related scientific experience OR
- Masters degree and 5 years of Engineering, Computer Science, Operations, Analytics, Data Science, or related scientific experience OR
- Bachelors degree and 7 years of Engineering, Computer Science, Operations, Analytics, Data Science, or related scientific experience OR
- Associates degree and 12 years of Engineering, Computer Science, Operations, Analytics, Data Science, or related scientific experience OR
- High school diploma / GED and 14 years of Engineering, Computer Science, Operations, Analytics, Data Science, or related scientific experience

**Preferred Qualifications:**

- Passion for data-driven business transformation and innovation
- Strong strategic thinking and problem-solving skills
- Ability to manage multiple priorities in a fast-paced global environment
- Experience working in manufacturing, operations, or supply chain domains
- Experience working within highly collaborative, matrixed, and global organizations
- Demonstrated ability to influence and drive alignment across technical and business teams

**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.

Process Development Senior 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 Senior Scientist**.

**What you will do**

Lets do this. Lets change the world. In this vital role you will join our Drug Substance Technologies - Synthetics (DSTS) group at either our Thousand Oaks, California or Cambridge, Massachusetts campus. In this dynamic role, the individual will drive innovative solutions to support manufacturing of therapeutic peptides at various stages of development; pre-IND through commercial production. The successful candidate will have a strong background and experience in industrialization of solid phase peptide synthesis, ideally complemented with experience in peptide purification, isolation, and characterization techniques. The individual will be highly motivated and team-oriented with a proven track record of scientific innovation and achievement.

**Responsibilities:**

- Work effectively with a diverse team of synthetic chemists, chemical engineers and analytical chemists to develop scalable synthetic processes utilizing solid phase peptide synthesis
- Drive technology innovation in solid-phase synthesis, purification, and characterization of synthetic peptides
- Support cGMP manufacturing and technology transfer to external contract manufacturers
- Advance enabling technologies to accelerate pharmaceutical development and to improve sustainability and process efficiency
- Ensure process performance through process understanding, modeling and characterization
- Contribute to drug substance development teams by providing experimental results, technical updates, documentation, data interpretation, recommendations, etc.
- Work cross-functionally to deliver regulatory documents and support regulatory filings
- Serve as a technical expert and keep current in the field of solid phase peptide synthesis
- Work independently in advancing projects and studies within required deadlines.

**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 scientific experience

OR

Bachelors degree and 5 years of scientific experience

**Preferred Qualifications:**

- Ph.D. in organic chemistry, biochemistry, or chemical engineering with expertise in synthetic peptide process development
- Extensive hands-on expertise in the synthesis and purification of synthetic peptides produced by solid phase synthesis
- Experience within the pharmaceutical/biotech industry developing solid phase peptide synthesis processes and scaling/transferring the process into GMP manufacturing
- Proficiency in analytical characterization techniques such as Hydrophobic Interaction Chromatography (HIC)-HPLC, Size Exclusion Chromatography (SEC), Liquid ChromatographyMass Spectrometry (LC-MS), Ion-Exchange (IEX), and Reversed Phase (RP)-HPLC.
- Familiarity with laboratory automation, data analysis and visualization techniques and tools
- Track record of peer-reviewed publications and research presentations
- Demonstrated ability to work within a dynamic and interdisciplinary environment to achieve results
- Excellent written and verbal communication skills, ability to multitask, effectively plan and follow through on complex 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.

Specialist Manufacturing Process Owner - Upstream / Downstream / Services

**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 bestworkalongside 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.

**Specialist Manufacturing Process Owner - Upstream / Downstream / Services (Multiple Positions)**

**Live**

**What You Will Do**

In this vital role, you will serve as a Process Owner within the Manufacturing Support organization atAmgenNorth Carolina (ANC). The Process Owner serves as a technical process steward and key interface between Manufacturing Operations and support organizations. This roleis responsible forsupporting manufacturing execution through technical process ownership, floor support, operational readiness activities, process governance, manufacturing change implementation support, and continuous improvement initiatives.

This position may support one of the following manufacturing areas depending on business needs and organizational assignment: Upstream Manufacturing, Downstream Manufacturing, or Manufacturing Services (Raw Material Dispensing and Solution Preparation).

- Serve as the technical process owner for assigned manufacturing processes, equipment, and unit operations.

- Provide manufacturing floor support, troubleshootingassistance, andhypercareduring routine manufacturing operations, process changes, startup activities, and first-time executions.

- Support operational readiness activities including water runs, dry runs, equipment readiness verification, and Electronic Batch Record (EBR) testingsupport.

- Partner with Manufacturing Operations to support reliable, compliant, and efficient manufacturing execution.

- Monitor process performance andidentifyopportunities for process optimization, operational improvement, and risk reduction.

- Support manufacturing-related change controls associated with process, equipment, procedural, and operational improvements.

- Author, revise, review, andmaintainmanufacturing SOPs, forms, and other GMP documentation.

- Ensure manufacturing processes are effectively translated into SOPs, manufacturing workflows, training materials, and associated digital manufacturing processes.

- Provide technical input to manufacturing risk assessments and support identification and mitigation of process, equipment, procedural, and operational risks.

- Participate in root cause analysis (RCA) activities and provide technical processexpertiseto support manufacturing investigations, major deviations, and quality events.

- Support CAPA applicability assessments, CAPA implementation activities, and CAPA effectiveness checks.

- Partner with Process Development to support process overviews, knowledge transfer activities, and facility fit assessments.

- Partner with Supply Chain, Manufacturing, and Engineering to support material readiness and Bill of Material (BOM) alignment, including single-use assemblies and consumables.

- Support MES and EBR activities by providing processexpertiseand manufacturing representation.

- Participate ininspectionreadiness activities and support audits asrequired.

- Appropriately escalate process, operational, quality, and compliance concerns.

**Win**

**What We Expect of You**

**Basic Qualifications**

- Doctorate degree and 2 years of biotechnology operations experience OR

- Master's degree in Engineering, Biology, Chemistry, Biochemistry, or related field and 4 years of biotechnology operations experience OR

- Bachelor's degree and 6 years of biotechnology operations experience OR

- Associate's degree and 10 years of biotechnology operations experience OR

- High school diploma / GED and 12 years of biotechnology operations experience

**Preferred Qualifications**

- Technicalexpertisein Upstream Manufacturing, Downstream Manufacturing, or Manufacturing Services (Raw Material Dispensing and Solution Preparation).

- Strong technical knowledge of drug substance manufacturing processes, equipment, and unit operations.

- Experience supporting GMP manufacturing operations in a biotechnology or pharmaceutical environment.

- Experience supporting manufacturing floor operations, troubleshooting, andhypercareactivities.

- Experience supporting operational readiness activities including water runs, dry runs, equipment testing, and startup support.

- Experience authoring and maintaining GMP documentation including SOPs and manufacturing procedures.

- Experience supporting manufacturing change controls and implementation activities.

- Experienceparticipatingin risk assessments, root cause analyses, investigations, and CAPA implementation activities.

- Experience supporting CAPA applicability assessments and effectiveness checks.

- Experience supporting Manufacturing Execution Systems (MES) and Electronic Batch Records (EBRs) within a GMP manufacturing environment.

- Knowledge of single-use technologies and Bill of Material (BOM) structures.

- Strong technical writing, communication, problem-solving, and organizational skills.

**Thrive**

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 through comprehensive benefits, career development opportunities, and a collaborative culture.

AV Production Technician

**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.

**AV Production Technician**

**What you will do**

Lets do this. Lets change the world. The AV Production Technician will support the planning, setup, operation, and delivery of high-quality live, hybrid, and virtual events across Amgens event spaces, auditoriums, control rooms, and digital collaboration environments. This role requires strong hands-on audio and video production skills, with particular emphasis on Dante audio workflows, NDI video workflows, streaming, webcasting, and virtual meeting support.

The ideal candidate is a collaborative, customer-focused technician who can work confidently in fast-paced production environments, support senior leaders and cross-functional teams, and deliver reliable, polished event experiences. This individual will partner closely with internal stakeholders, Customer Care and Experience teams, vendors, event owners and event coordinators to ensure every production is technically sound, well-executed, and aligned to business needs.

**Responsibilities:**

- Support the end-to-end technical execution of live, hybrid, and virtual events, including meetings, town halls, webcasts, executive events, auditorium productions, and large-scale campus events.
- Operate, configure, and troubleshoot AV production systems, including audio consoles, video switchers, playback systems, cameras, microphones, encoders, decoders, displays, and control room equipment.
- Manage and support Dante audio networks, including audio routing, device configuration, signal flow validation, monitoring, and troubleshooting.
- Manage and support NDI video workflows, including NDI-enabled cameras, encoders/decoders, routing, discovery, software tools, and network-based video transport.
- Provide technical support for streaming and webcasting platforms, including event setup, testing, monitoring, and live support.
- Support virtual and hybrid meeting technologies, including Webex, Microsoft Teams, and Zoom, ensuring strong audio/video quality and a smooth user experience.
- Serve in multiple live production roles as needed, such as Audio Technician, Video Technician, Virtual Meeting Operator, Graphics Operator, Playback Operator, Streaming Technician, or Technical Support.
- Perform pre-event checks, equipment readiness assessments, signal testing, room validation, and quality control to ensure successful event delivery.
- Partner with event owners, coordinators, executives, presenters, and technical teams to understand event goals and translate them into effective production plans.
- Maintain auditoriums, and control room systems, including video walls, audio systems, control systems, networked AV devices, and production equipment.
- Troubleshoot issues quickly and professionally during live events, escalating when needed while maintaining a calm and solutions-focused presence.
- Support continuous improvement of AV production spaces, workflows, documentation, equipment standards, and operational procedures.
- Coordinate with vendors and internal technical teams for equipment repairs, upgrades, installations, and event-specific production needs.
- Deliver a high level of customer service while supporting a wide range of internal clients, including senior executives and business-critical stakeholders.

**What we expect of you**

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

**Basic Qualifications:**

Bachelors degree

OR

Associates degree and 4 years of engineering experience and/or event production experience

OR

High school diploma / GED and 6 years of engineering experience and/or event production

**Requirements:**

- Hands-on experience supporting live, hybrid, and virtual event production in a corporate, enterprise, auditorium, broadcast, or similar professional environment.
- Strong working knowledge of professional audio systems, including microphones, wireless systems, mixers/consoles, DSPs, signal flow, gain structure, and live audio troubleshooting.
- Practical experience with Dante audio, including device setup, routing, patching, monitoring, and troubleshooting.
- Strong working knowledge of professional video systems, including cameras, switchers, displays, video playback, capture devices, signal routing, and production workflows.
- Practical experience with NDI video, including NDI software, hardware devices, IP-based video workflows, and troubleshooting.
- Experience supporting streaming, webcasting, and virtual event platforms.
- Experience supporting collaboration platforms such as Webex, Microsoft Teams, and Zoom in live or executive-facing environments.
- Strong troubleshooting skills with the ability to remain composed and effective under pressure.
- Excellent customer service skills and the ability to communicate clearly with both technical and non-technical stakeholders.
- Strong organizational skills, attention to detail, and ability to manage multiple priorities in a fast-paced environment.
- Self-directed, proactive, and comfortable learning new technologies, tools, and production workflows.

**Preferred Qualifications:**

- Experience supporting live events, executive meetings, webcasts, or corporate AV production for large enterprise environments.
- Experience with platforms and tools such as Webex Events, Microsoft Teams Live Events/Town Halls, Socio, Kaltura, Zoom Events/Webinars, VizRT, or similar production and streaming technologies.
- Experience with production switchers such as Analog Way Aquilon or other industry-standard video switching platforms.
- Experience with video systems like Lightware, Panasonic PTZs, NDI, Epiphan Pearl 2, Kipro Ultra, Atomos, Perfect Cue Clickers, Speaker Timers, and more
- Experience with audio systems such as Shure, Yamaha CL/QL and DM7 consoles, Biamp, or similar professional audio platforms.
- Experience supporting Crestron-controlled rooms, auditoriums, video walls, AV-over-IP systems, or enterprise collaboration spaces.
- Knowledge of Office 365 collaboration tools, Outlook, Teams, SharePoint, Box, or other enterprise productivity platforms.
- Experience with PC and Mac computers
- Familiarity Agile practices, ticketing systems, or enterprise IT support environments.

**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.

Senior Manager Manufacturing Programs- Process Owner Organization

**HOW MIGHT YOU DEFY IMAGINATION?**

If you feel like youre part of something bigger, its because you are. At Amgen, our shared missionto serve patientsdrives all that we do. It is key to our becoming one of the worlds leading biotechnology companies. We are global collaborators who achieve togetherresearching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. Its time for a career you can be proud of.

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 single use 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 Manager Manufacturing Programs**

**Live**

**What you will do**

We are seeking a Senior Manager ofManufacturing Programsto lead the Process Owner organization within Manufacturing Support at ANC. This leadership role is responsible for providing technical process stewardship, manufacturing support, process governance, and manufacturing changecontrolsupport for Upstream, Downstream, and Services Drug Substance Unit Operations.

The Process Ownerteamserves as the technical process steward for manufacturing operations, partnering closely with Manufacturing Operations and cross-functional support functions to ensure manufacturing processes are effectively governed, implemented, maintained, and continuously improved throughout their lifecycle.

Process Owners serve as the primary technical liaisons between Manufacturing Operations and support organizations including Quality, Engineering, Process Development, Commissioning & Qualification (C&Q), Supply Chain, and Digital Manufacturing. Through floor presence,hypercaresupport, process ownership, operational readiness activities, and manufacturing change implementation, the team enables reliable, compliant, and efficient manufacturing execution.

The Senior Manager will lead a growing organization of Process Owners responsible for process ownership, floor support andhypercareactivities, operational readiness assessments, dry and water run execution, electronic batch record implementation support, manufacturing change implementation, BOM support, and procedural governance. This role will also be responsible for expanding organizational capabilities, including establishing and leading a swing-shift Process Owner team to provide enhanced operational support and manufacturing coverage.

**What You Will Do**

- Lead and develop the Process Owner organization responsible for providing technical process stewardship and manufacturing support for Upstream, Downstream, and Services Drug Substance Unit Operations.

- Provide direct management, coaching, mentoring, and career development for Process Owners.

- Develop and implement a swing-shift Process Owner organization to provide expanded manufacturing support and floor coverage.

- Foster a culture of safety, quality, compliance, accountability, collaboration, operational excellence, and continuous improvement.

- Provide strategic leadership for process ownership, operational readiness, manufacturing change implementation,manufacturing procedures, manufacturing CAPAs,and technical process stewardship.

- Coordinate with site scheduling to ensure Process Owners provide timely hyper-care support and technical assistance during manufacturing campaigns, startup activities, process changes, first-time executions, and routine operations.

- Serve as the primary interface between Manufacturing Operations and support organizations including Quality, Engineering, Process Development, C&Q, Supply Chain, and Digital Manufacturing.

- Oversee execution of dry runs, water runs, engineering runs, and operational readiness activitiessupporting manufacturing.

- Own manufacturing-relatedCAPAs andchange controls associated with process, procedural, and operational improvements.

- Provide leadership andinputfor electronic batch record (EBR) and manufacturing execution system (MES) implementation activities impacting manufacturing operations.

- Partner withTechnologyteams to ensure manufacturing processes are effectively translated into digital workflows and manufacturing execution platforms.

- Partner with Supply Chain organizations to ensure manufacturing processes, material strategies, and Bill of Materials(BOM) support efficient manufacturing execution.

- Provide process ownership oversight for BOM creation, maintenance, and updates associated with manufacturing process changes.

- Ensure creation, revision, maintenance, and periodic review of GMP documentation supporting manufacturing operations.

- Drive strategic initiatives to improve process reliability, manufacturing efficiency, operator experience, and operational performance.

- Support inspection readiness activities and represent the Process Owner organization during audits and regulatory inspections as required.

**Win**

**What We ExpectofYou**

**Basic Qualifications:**

Doctorate degree and 2 years of biotechnology or pharmaceutical industry experience

OR

Masters degree and 6 years of biotechnology or pharmaceutical industry experience

OR

Bachelors degree and 8 years of biotechnology or pharmaceutical industry experience

OR

Associates degree and 10 years of biotechnology or pharmaceutical industry experience

OR

High school diploma / GED and 12 years of biotechnology or pharmaceutical industry experience

In addition to meeting at least one of the above requirements, you must have a minimum of 2 years experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation or resources. Your managerial experience may run concurrently with the required technical experience referenced above

**Preferred Qualifications:**

- 8+ years related work experience in biotechnology or pharmaceutical manufacturing with progressively increasing responsibility.

- Prior people leadership experience managing and developing technical teams.

- Strong understanding of GMP manufacturing operations supporting Upstream, Downstream, and Services Drug Substance Unit Operations.

- Experience with process ownership, manufacturing support, and technical process stewardship.

- Experience supporting digital manufacturing systems, electronic batch records (EBRs), manufacturing execution systems (MES), and associated process implementation activities within a GMP manufacturing environment.

- Experience authoring, approving, and governing manufacturing SOPs and GMP documentationwithinQuality Systems (i.e. Veeva,Documentum, etc.).

- Experience leading manufacturingCAPAs/change controls and implementation activities.

- Experience supporting operational readiness activities, including dry runs, water runs, process implementation, and startup support.

- Experience partnering with Supply Chain organizations to support BOM management, material readiness, and manufacturing execution.

- Excellent organizational, written, verbal communication, and cross-functional leadership skills.

Specialist Manufacturing New Product Introduction (NPI):Downstream Readiness

**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,experienceand 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 bestworkalongside 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.

**Specialist Manufacturing New Product Introduction (NPI): Downstream Readiness**

**Live**

**What youwill do**

Letsdo this.Letschange the world.In this vital role you will communicate and interface between the GMP manufacturing teams in theAmgen North Carolina (ANC) Biologics Drug Substance ManufacturingplantandProcessDevelopment scientific groups.As part of ANCs Manufacturing Supportteam, this positionis responsibleforensuring new products are successfully introduced intoANCsbiologicsmanufacturingfacility.It is ahighly visible role across the site with the core responsibility ofhosting cross-functional meetings todrive totimelines to support the tech transfer of the program into the facility.This role will also offer the opportunity to propose,participate, and lead team improvement initiatives to drive improved productivity and scheduling accuracy.

Responsibilities:

- New Product Introduction(NPI)leadcoordinatingwithManufacturing, Process Development,Supply Chain, Planning, Facilities and Engineering, Quality, and other teamsto introduce new Drug Substance products and/or advanced technologies into the plantusingproject management tools.

- Technical expert who leads orparticipatesin projects, ensuring that production documents areaccurateand up to date.

- Support Manufacturing in troubleshooting, problem-solvingand RCAs. Support CAPA development to prevent error recurrence.

- Owns New Product Introduction(NPI)Change Controlsand collaborates with stakeholders to drive on-time completion.Respondsto regulatory questions and/or audit findings.

- Champions Lean Transformation and OEinitiatives,facilitatesthe drive towards continuous improvement in the plant,and tracks progress on a plant level.

**Win**

**What we expectofyou**

We are all different, yet we all use our unique contributions to serve patients. Themanufacturingprofessional weseekhas a biologics DSmanufacturing background withstrongcross-functional project managementandcommunicationskillsas well asthebelowqualifications.

**Basic Qualifications:**

- High school diploma / GED & 10 years of biotechnology operations experience OR
- Associates degree & 8 years of biotechnology operations experience OR
- Bachelors degree and 4 years of biotechnology operations experience OR
- Masters degree in chemistry, biology, or engineering & 2 years of biotechnology operations experience OR
- Doctorate degree

**Preferred Qualifications:**

- Degree in Chemical Engineering, Industrial Engineering, Biology, or Biochemistry.

- Excellentcross-functionalproject management, meeting facilitation, andtechnical writing skills.

- Experience in GMPmanufacturingoperations.

- Strong technical knowledge of drug substance processingin Cell Culture or Purification(chromatography, filtration, buffer compounding) and a broad understanding of related disciplinary areas in bioprocessing.

- Ability to organize,analyzeand interpret technical data through trend analysis, forecasting, modeling, etc.

- Ability to effectively communicate complex technical information with internal and external colleagues of varying organizational levels in both presentation and technical writing forms.

- Ability to coach,mentorand/or cross train colleagues within core technical areas.

- Background in lean manufacturing methodologies and operational excellence.

**Thrive**

**What you can expectofus**

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 annual base salary range for this opportunity in the U.S. is provided below.

In addition to the base salary, Amgen offers a Total Rewards Plancomprisinghealth 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 forfield 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**

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 areprovidedreasonable accommodation toparticipatein 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.

**#AmgenNorthCarolina**

Sr. Data Scientist - Process Modeling

**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.Data Scientist - Process Modeling**

**What you will do**

Lets do this. Lets change the world. In this vital role you will join the Digital Process and Systems Analysis group within Process Development plays a key role in providing data infrastructure, platforms, and analytics to support engineering teams across our network, ensuring state-of-the-art data insights to drive innovation and efficiency for the commercialization and optimization of Amgens pipeline. This group also supports key priorities and the development of strategies for digital process development for both biologic and synthetic moieties.

This position is part of a team advancing biologics drug-substance modeling and the digitization of tech-transfer workflows. As new modeling capabilities are developed and information is parameterized, opportunities abound to deploy modeling tools to enable early insights and phase-appropriate decision-making. These capabilities support drug substance development, technology transfer, manufacture, and life-cycle management across Amgens global network of manufacturing and development sites.

This role will contribute to the success of Drug Substance Technology organization by helping to digitize workflows to drive improvements in technology transfer timelines and ensure right-first-time success. As a Sr. Data Scientist, you will evaluate and improve Amgens digital assets, collaborating as part of a multi-disciplinary team of scientists and engineers on a wide range of problems. The position will lead to solutions for open-ended no single right answer challenges, including modeling, data pipelines, and visualizations to support drug substance development, tech transfer, and manufacturing. The Sr. Data Scientist will also be responsible for determining, defining, and tracking performance improvements.

**Responsibilities**:

- Leverage tech-transfer and process-modeling domain knowledge to drive implementation of digital technologies
- Digital Product Ownership of tech-transfer digital applications, focused initially on expansion of digital process-modeling for the DS network
- Change management to integrate tech transfer digital applications into product teams
- Development of data products to enable FAIR data for tech transfer/NPI
- Enable AI Agentic workflows for DST modeling assets
- Collaborate with digital product teams to build and integrate modeling assets into business processes for DST
- Interact cross-functionally with a wide variety of people and teams. Work closely with engineers to identify opportunities for process design improvements for Amgen products
- Make business recommendations (cost-benefit, forecasting, scenario analysis) with effective presentation of findings to varied levels of stakeholders
- Contribute to establishing a robust data science strategy by providing recommendations related to process monitoring, data engineering, analytic platforms, analysis plans, and other relevant areas of data science

**What we expect of you**

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

**Basic Qualifications:**

Doctorate degree

OR

Masters degree and 2 years of Data Science or Engineering experience

OR

Bachelors degree and 4 years of Data Science or Engineering experience

OR

Associates degree and 8 years of Data Science or Engineering experience

OR

High School diploma or GED and 10 years of Data Science or Engineering experience

**Preferred Qualifications:**

- MS degree or doctorate in an engineering or scientific field with demonstrated capability in application of data science.
- Chemical Engineering modeling, drug-substance, tech-transfer experience
- 3+ years of work experience in biotechnology role (e.g. process engineer, scientist, data scientist)
- Experience with AGILE software development methodologies
- Experience with Databricks, coding languages (Python, SQL), AI Tools (Chat GPT, Codex, GenieCode), React, and BI tools (Spotfire/Tableau/Power BI)
- Experience in developing AI applications for process development workflows and integrating AI solutions into process development business processes
- Experience with process modeling for cell-culture, harvest,and purification scale-up
- Demonstrated performance in application of digital tools to solve analytical problems
- Demonstrated effective written and verbal communication skills
- Demonstrated leadership and self-direction. Demonstrated willingness to both teach others and learn new techniques as well as manage team members and deliverables.

**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.

Process Development Principal 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 Principal Scientist**

**What you will do**

Lets do this. Lets change the world. In this vital role you will joining Amgens Attribute Sciences (AS) department within the Process Development (PD) organization defines the favorable quality characteristics of the therapies it produces and optimizes state-of-the-art analytical tools to guide that development. The Pivotal PD organizations focus is developing and commercializing robust manufacturing processes across a wide range of therapeutic modalities, including (but not limited to) synthetic medicines (oligonucleotides and small molecules).

In this vital role as an Attribute Sciences team lead and group lead you will work to provide strategic analytical leadership to teams developingcommercialmanufacturing processes for synthetic and hybrid molecules and collaborate closely with Drug Substance, Drug Product and Product Quality colleague

- Lead all attribute and analytical aspects of a program in pivotal clinical process development while working cross-functionally within a Product development team
- Define analytical control strategies and implement methodologies for development of late phase clinical programs including analytical method development and optimization
- Lead method transfer and support cGMP manufacturing activities at internal manufacturing, and contract manufacturing and testing sites
- Author technical reports and analytical Chemistry, Manufacturing and Controls (CMC) sections in regulatory documents. Answer analytical and product quality questions from health authorities
- Drive product characterization in support of process comparability studies, regulatory filings, regulatory questions, and reference standard qualification
- Provide expertise and evaluation of Amgens platform and analytical technologies, helping to drive innovation and efficiency within Process Development
- Help to define strategies that improve the effectiveness and efficiency of the Attribute Sciences department
- Maintain current in the analytical development field including literature and technology development for cutting edge and regulatory driven activities and apply this knowledge to the evaluation and development of new methodologies
- Recognized as a scientific resource in area of expertisewho can provide mentorship to junior staff.

**What we expect of you**

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

**Basic Qualifications:**

Doctorate degree PhD OR PharmD OR MD \[and relevant post-doc where applicable\] and 3 years of \[Job Codes Discipline and/or Sub-Discipline\] experience

OR

Masters degree and 6 years of Scientific experience

OR

Bachelors degree and 8 years of Scientific experience

**Preferred Qualifications:**

- PhD with 3+ plus years of industry experience.
- Strong understanding of small molecule analysis including chromatographic and spectroscopic techniques with an emphasis toward separation science, Process Analytical Technologies (PAT) for process understanding and process control, structure elucidation and solid-state characterization
- Knowledge of analytical method development and testing requirements toward solid oral dosage support (immediate and controlled release solid dosage forms, liquid formulation or lyophilized formulation), including dissolution method development.
- Solid understanding of Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP) requirements and their application in a phase appropriate manner
- Hands on experience in development, validation, transfer and remediation of methods for in-process, release and stability testing
- Knowledge of the major Pharmacopeia and International Conference on Harmonization (ICH) / Food & Drug Administration (FDA) guidance documents related to analytical method transfer and validation, impurities, genotoxic impurities, early phase development.
- Experience in technical transfer for non-GMP and GMP production and testing to external contract organizations
- Ability to multitask managing deliverables on complex projects against timelines
- Strong leadership, problem solving, decision making and communication skills with the ability to work cross-functionally and globally within CMC teams to deliver results
- Excellent technical writing skills and attention to details 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.

Senior Process Engineer - Solution Prep, Upstream, and Downstream

**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.

**SeniorProcessEngineer-Solution Prep,Upstream,andDownstream**

**What youwill 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.This role will develop domainexpertiseand system ownershipto supportprocessoperations, focusing onSolution Prep,Upstream,andDownstreamProcess engineering and plant equipment.

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

- Support thedesign andbuildof manufacturingequipmentsystems byaligningdesign reviewprocessesand documentswith site requirements, including equipment design and sizing, architecture and electricaldistribution, and piping and instrumentation diagrams.

- Supportfactoryacceptancetestingworking in partnershipwith global engineeringduringsiteinstallation,including reviewing protocolsandresolving punch list items.

- Work withcapitalproject teamto ensure systems are installed andoperatingsafelyandcomply withpertinent environmental health/safety practice,rulesand regulationsas well as Amgen global engineering requirements.Ensurethat systems are installed per the designrequirements.

- Executeand guidethe commissioning and validationof systemsto ensure their operational capabilityis alignedwithmanufacturing requirements andGMPregulationand on-time project delivery.Supportexecution of engineering and performance qualification runswhile providinghypercaresupport as needed.

- Perform engineering assessmentsfor plant equipment operations,implementing equipment modifications, and supporting engineering runsin support of new product/technology introductions asrequired.

**Site Operations:**

- Responsible system ownerforSolution Prep,Upstream,andDownstreamDrug substanceprocess equipment, areas, and systems providingend-to-endsupport for operations.

- 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 ofprocess equipmentas applicable.

- Leadidentifyingand implementing engineering-based improvements or upgrades toprocessequipmentsystems.This may include developing business cases for improvements,identifyingdesign requirements, and translating these requirements intoprocessequipment/system design, specifications, and supporting the construction, startup, and validation of equipment.

- Developmastermaintenance programsfor 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 theprocessequipment.

- Providetechnical masteryandproblem-solvingleadershiptoproactivelyreduce production downtime. Thisincludes leadingtechnical root cause analysis and implementation of corrective/preventiveactions for families of systems.

- Leadnew product/technology introductions by performing engineering assessments,equipment performance risk assessments,identifyinggaps and owning their remediation,implementing equipment modifications, and supporting engineering runs.

- Provide rotational on-call support and/or shift support based on business needs to ensure24x7 day-to-dayreliability of Solution Prep, Upstream and Downstream systemsfor plant operations.

- On-site and up to10% domestic/international travel.

**What we expectofyou**

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

**Basic Qualifications:**

Doctorate degree

OR

Mastersdegree and 2 years of Engineering experience

OR

Bachelorsdegree and4years ofEngineeringexperience

OR

Associatesdegree and8years ofEngineeringexperience

OR

High school diploma / GED and10years ofEngineeringexperience

**Preferred Qualifications:**

- Degree in Chemical or Mechanical Engineeringor similar engineering discipline.

- 6+years'of relevant work experience with 5+ years' experience in Biopharmaceuticaloperations/manufacturing environment

- Direct knowledge of design and troubleshooting with GMP Biopharmaceutical Productionfacility equipment/systemswith direct experience withSolution Prep,Upstream,andDownstreampurification equipment suchasweigh and dispense equipment, solution preparation vessels,cell culture reactors, centrifugation, chromatography,viralfiltration skids,andUFDFskidsas 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 Tech Transfer, Process Design, and Commissioning & Qualification.

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

- Understanding ofsafety requirements working in a GMP Biopharmaceuticalproductionfacility.

- 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 asrequiredto support 24/7 operations.

- Ability for domestic/international travel.

**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.

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

**careers.amgen.com**

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 Engineer - Solution Prep, Upstream, and Downstream

**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.

**ProcessEngineer-Solution Prep,Upstream, andDownstream**

**What youwill 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 as well as developing domain expertise tosupport operations upon start-up.

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

- Support the commissioning and qualification ofmanufacturingsystems in alignment with GMP requirements and interact with regulatory inspectors.

- Ensuresystemsare installed andoperatesafelyandcomply withpertinent environmental health/safetypractice,rulesand regulations.

- Support commissioning and qualification of systemsto ensure their operational capabilityis alignedwithmanufacturing requirements andGMPregulations.

- Interact with regulatory inspectorsas a manufacturing systems owner to communicate anddemonstrateappropriate regulatorycomplianceofoperating systems.

- Assistwithnew product/technology introductions by performing engineering assessments,implementing equipment modifications, and supporting engineering runs.

**Site Operations:**

- Provide systemsupportforbiopharmaceutical process equipment.Assistinidentifyingand implementing engineering-based improvements or upgrades to equipment or facility systems.

- Support the developmentofbusiness cases for improvements,identification ofdesign requirements, and translation ofthese requirements into process equipment/system design, specifications, and supporting the construction, startup, and validation ofimprovements.

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

- Providesystem guidance toidentifyperformance risks and implement risk reduction strategies.

- Provideproblem solving support to reduce production downtime. Thisincludessupporting technical root cause analysis and implementation of corrective/preventiveaction.

- Provide rotational on-call supportand/or shift supportbased on business needstoensure24x7 day-to-dayreliability ofSolution Prep,Upstream and Downstream systemsfor plant operations.

- On-site and up to10% domestic/international travel.

**What we expectofyou**

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

**Basic Qualifications:**

Masters degree

OR

Bachelorsdegree and 2 years ofEngineeringexperience

OR

Associatesdegree and 6 years ofEngineeringexperience

OR

High school diploma / GED and 8 years ofEngineeringexperience

**Preferred Qualifications:**

- Bachelors degree in Chemical or Mechanical Engineeringor similarengineerdiscipline.

- 3+years'of relevant work experience with2+ years' experience in Biopharmaceuticaloperations/manufacturing environment

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

- Ability to analyze problems, develop and propose engineering solutions in a scientificmanner using data-driven techniques and analyses (e.g., Data Analytics, Root CauseAnalysis (RCA), Statistical Process Control (SPC), Six Sigma, Predictive Maintenance, etc.)

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

- Experience applying engineering principles to the design and implementation of systemmodifications, introduction of new processes, and the oversight of capital projects

- Understanding of capital projects in a GMP Biopharmaceutical Production facility includingprocurement, construction, startup, and validation

- Understanding ofsafety requirements working in a GMP Biopharmaceutical Productionfacility.

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

- Collaborativeteammateprepared to work in and embrace ateam basedenvironment thatrelies on communication for effective decision-making

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

- Work schedule flexibility asrequiredto support 24/7 operations, requiring occasionalafterhoursengineering coverage

- Ability for domestic/international travel.

**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.

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

**careers.amgen.com**

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.