Engineering

Amgen

Associate Engineer

**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, 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 Engineer**

**What you will do**

Lets do this. Lets change the world. In this role the Associate Engineer reports to the Senior Manager of the Engineering group. The position is responsible for providing daily process, equipment, maintenance, and reliability engineering support at the Amgen Rhode Island site.

**Scope of Responsibility**

- Apply engineering principles to support the operation, maintenance, and improvement of process systems used in commercial and clinical manufacturing.

- Provide technical and field support to troubleshoot process equipment and control issues, identify causes of poor performance, and implement solutions.

- Coordinate with Manufacturing, Process Engineering, Process Development, Utility Operations, Maintenance, Quality Assurance, and Validation to resolve issues and implement operational improvements.

- Organize and analyze data, then present results and recommendations for operational issues, maintenance activities, and engineering projects.

- Support the design, construction, startup, commissioning, and qualification of new or modified systems, completing assigned work under the direction of lead engineers and within schedule and budget constraints.

- Improve equipment and maintenance information in Maximo, including equipment records, job plans, spare parts, safety information, and preventive maintenance schedules.

- Support maintenance planning and execution, and advance condition-based and predictive maintenance practices using data analytics where applicable.

- Investigate abnormal conditions through Deviation and INCA processes, with guidance appropriate to the scope and complexity of the issue.

- Work with engineers and technicians on ongoing operations and projects. Communicate progress, issues, and proposed solutions to supervisors and support teams.

- Participate in a rotating 24/7 on-call schedule to support process systems, including nights, weekends, and holidays as needed

The onboarding phase for this role will last approximately 26 weeks, during which time successful incumbents will become familiar with site operations, engineering systems, quality processes, safety expectations, and cross-functional ways of working. This is a days-based role, generally aligned to an administrative schedule, with flexibility required to support business needs, critical operations, shutdowns, investigations, or occasional off-hours issues as necessary.

**What we expect of you**

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

**Basic Qualifications**

- High school diploma / GED and 6 years of engineering experience OR

- Associates degree and 4 years of engineering experience OR

- Bachelors degree

**Preferred Qualifications**

- Bachelors degree in engineering or related technical field

- Strong written and verbal skills and the ability to work with minimum direction.

- Demonstrated interpersonal and facilitation skills and ability to work in a collaborative team-based environment.

- Ability to apply analytical skills to evaluate and interpret sophisticated problems using multiple sources of information.

- Ability to function within cross-functional teams and embrace a team-based environment.

- Experience with Mammalian Cell Culture, Protein Purification, Clean Utilities, CIP, SIP, Production Services and non-GMP Utilities.

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

**What you can expect of us**

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

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

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

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

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

- Stock-based long-term incentives

- Award-winning time-off plans

- Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.

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

**careers.amgen.com**

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

**Application deadline**

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

**Sponsorship**

Sponsorship for this role is not guaranteed.

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

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

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

Rhode Island

Undergrad Co-op - Electrical Engineering (Jan - Mar 2027)

**Join Amgens Mission of Serving Patients**

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

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

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

**Undergrad Co-op - Electrical Engineering (Jan - Mar 2027)**

**What You Will Do**

Lets do this. Lets change the world. During this program, you will be reporting to a Manager of Maintenance, this position is responsible for performing tasks related to electrical system operation and maintenance activities throughout the Amgen Rhode Island (ARI) site.

Specific duties may include:

- Gain experience operating a large-scale production facility by shadowing technicians in various functions within the Facilities & Engineering department to operate, maintain, and sustain all major electrical equipment on site
- Taking part in improvement projects related to the electrical systems at ARI through supporting day-to-day operations to ensure a safe, compliant, effective, efficient, and cost appropriate utility operations at ARI
- Assist Amgen electrical group in troubleshooting and repair of equipment and systems
- Ensure activities are accomplished in a safe manner
- Assist Amgen electrical group to ensure work order documentation is completed accurately and completely
- Identify opportunities to learn new skills and actively participate in development that will improve overall knowledge
- Collaborate with Facilities & Engineering peers within the Amgen network

**Program Eligibility Requirements**

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

**What We Expect of You**

We are all different, yet we all use our unique contributions to serve patients. The collaborative individual we seek is a hard worker with these qualifications:

**Basic Qualifications:**

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

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

**Preferred Qualifications**

- Complete/ongoing coursework in the following areas:
  - Mechanical engineering technology
  - Electrical engineering technology
  - Electronics/instrumentation/controls systems and automation
  - Welding technology
  - HVAC/refrigeration
  - Plumbing/pipefitting
- Knowledge and understanding of working in a highly regulated function
- Equipment troubleshooting skills
- Knowledge of computerized maintenance management systems
- Ability to understand drawings, P&IDs and equipment schematics and wiring diagrams
- Ability to follow written procedures and job instructions to operate and maintain systems and equipment

**What You Can Expect of Us**

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

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

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

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

**careers.amgen.com** Please search for Keyword R-257526

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

**Application deadline**

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

**Sponsorship**

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

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

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

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

Senior Engineer

**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 Engineer**

**What you will do**

Lets do this. Lets change the world. In this vital role you will work with the Sr. Engineering Manager and will provide engineering support for the Drug Substance facilities.

- Identify, support, and/or lead implementation of engineering based improvements or upgrades to the equipment or facility systems. This may include development of business case for improvement and identification of design requirements and then translation of requirements into process equipment/system design, specification and supporting the construction, startup, and validation of equipment.
- Directing and coordinating equipment maintenance as necessary to ensure systems are in proper working order
- Ensure necessary commissioning and qualification of systems is completed and interact with inspectors
- Develop metrics-based performance focused on the maintenance systems effectiveness and operating level performance.
- Providing troubleshooting support to reduce production downtime. This will involve leading and/or supporting technical root cause analysis and implementation of corrective/preventive action
- Support new product/technology introductions by performing engineering assessments, implementing equipment modifications, identifying spare parts, job plan development and supporting engineering runs.
- Ensure systems are installed and operating safety and align with pertinent environmental health/safety practice, rules and regulations
- Responsible for determining appropriate CAPAs, action plan development, QMTS data entry, owns the record, initiate child CAPAs and CAPA EVs, timely closure and responses, provision of technical data and reports.
- Use tools and techniques of continuous improvement wherever possible. Establish equipment monitoring parameters and control limits. Routinely provide updates on metrics. Provide 2nd tier trouble shooting to support ops and maintenance groups as follow on from tier 1 initial problem solving. Change over reduction projects. Failure trending
- Up to 10% domestic travel

**What we expect of you**

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

**Basic Qualifications:**

Doctorate degree

OR

Masters degree and 2 years of engineering experience

OR

Bachelors degree and 4 years of engineering experience

OR

Associates degree and 8 years of engineering experience

OR

High school diploma / GED and 10 years of engineering experience

**Preferred Qualifications:**

- Bachelors degree in Biotechnology, Industrial, Chemical or Mechanical Engineering
- 6+ years' of relevant work experience with 5+ years' experience in Biopharmaceutical operations/manufacturing environment
- Experience working in a regulated environment (e.g. cGMP, OSHA, EPA, etc.) and familiarity with GMP quality systems/processes such as change control, non-conformances, corrective and preventative actions, and qualifications/validation
- Direct knowledge of design and troubleshooting with GMP Biopharmaceutical Production facility equipment/systems such as cell culture reactors, chromatography, filtration, filling, lyophilization, inspection, device assembly, 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 scientific manner using data-driven techniques and analyses (e.g., Root Cause Analysis (RCA), Statistical Process Control (SPC), Six Sigma, Predictive Maintenance, etc.)
- Experience applying engineering principles to the design and implementation of system modifications, introduction of new processes, and execution of capital projects
- Understanding of the execution process of capital projects in a GMP Biopharmaceutical Production facility including procurement, construction, startup, and validation
- Understanding of safety requirements working in a GMP Biopharmaceutical Production facility.
- Independent, self-motivated, organized, able to multi-task in project environments, and skilled in communication, facilitation, and collaboration
- Team player prepared to work in and embrace a team based culture that relies on collaboration for effective decision-making
- Strong leadership, technical writing, and communication/presentation skills
- Work schedule flexibility to support 24/7 operations, requiring occasional after-hours engineering coverage as required from time to time

**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

Project Controls Senior Manager - Scheduler

**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. Amgen is advancing a broad and deep pipeline and portfolio of medicines to treat heart disease, obesity and obesity-related conditions, rare diseases, inflammatory conditions and cancer. As a member of the Amgen team, youll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.

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

**SENIOR MANAGER PROJECT CONTROLS - SCHEDULING**

**What you will do**

Lets do this. Lets change the world. In this vital role you will lead the Planning and Scheduling function supporting Amgen's capital project portfolio. This role provides organizational leadership for a team of planners and schedulers while establishing standardized planning processes, portfolio governance, and scheduling best practices across multiple capital programs. The leader partners with Project Management, Engineering, Construction, Procurement, CQV, Finance, Manufacturing, Site Operations, and Regulatory organizations to ensure projects are planned, executed, and reported consistently throughout the project lifecycle. In addition to maintaining technical excellence in project scheduling, the leader is responsible for developing talent, managing organizational resources, driving standardization and continuous improvement initiatives, implementing digital planning solutions, and providing portfolio-level analytics that support executive decision making.

- Lead the Planning and Scheduling organization and portfolio.
- Supporting Amgen's capital project portfolio, ensuring standardized planning practices, portfolio governance, and successful execution across multiple concurrent capital projects.
- Executive and network reporting performance dashboards within capital project portfolio.
- Support the development of integrative master schedules from planning to operational readiness through licensure.
- Establish staffing strategies and optimize resource allocation across multiple projects.
- Champion digital planning solutions including Primavera P6, Planisware, AI-enabled planning tools, and reporting platforms.
- Partner closely with Project Managers and Project Controls teams to support successful project delivery.
- Build strong relationships with internal stakeholders across all organizational levels.
- Develop standard methodology for earned value management and risk management.
- Work closely with various disciplines in project teams to ensure the accuracy and completeness of the schedules.
- Manage the Planning and Scheduling organization supporting the capital portfolio.
- Lead planning governance across all assigned projects.
- Mentor planners and project controls professionals.
- Manage contractor scheduling requirements and performance.
- Coordinate with all organizational subject matter experts to ensure accurate reporting.
- Collate project-level schedule reporting to produce program-level schedule reporting.
- Coordinate the alignment of the project-level schedules with the Master Program Schedule
- Provide data required for Earned Value Management
- Perform impact analyses and schedule updates as required.
- Oversee and proactively provides guidance to project-level schedule consultants.
- Perform schedule forecasting and predictability.
- Incorporate schedule Change Orders in coordination with Program Change Management
- Lead implementation of schedule AI-enabled planning tools.
- Drive digital transformation initiatives within Project Controls.
- Develop data-driven planning dashboards using Power BI and Planisware.
- Promote automation and predictive scheduling methodologies.

**What we expect of you**

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

**Basic Qualifications:**

- High school diploma / GED and 12 years of Engineering and capital projects delivery
- experience OR
- Associates degree and 10 years of Engineering and capital projects delivery
- experience OR
- Bachelors degree and 6 years of Engineering and capital projects delivery experience OR
- Masters degree and 4 years of Engineering and capital projects delivery experience OR
- Doctorate degree and 2 years of Engineering and capital projects delivery experience

**Preferred Qualifications:**

- Experience in capital project delivery. managing Engineering or Construction in project controls across estimating, cost control, scheduling, and compliance
- Expertise in planning and scheduling while possessing proven leadership capabilities to execute capital construction projects.
- Experience managing integrated master schedules, developing planning standards, mentoring planning professionals, and leading cross-functional organizations.
- Effective communication, organizational leadership, and executive presentation skills are essential, along with the ability to influence stakeholders across all organizational levels.
- Computer Systems: Primavera P6 expert, MS Project and Planner, Excel, Smart Planning, Smartsheets, Power Bi

**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 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. We make all employment decisions without regard to race, color, religion, sex or any other characteristic protected by applicable law.

We provide reasonable accommodations to applicants and employees with disabilities, consistent with legal requirements. Please contact us to request accommodation.

Ohio

Project Controls 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. Amgen is advancing a broad and deep pipeline and portfolio of medicines to treat heart disease, obesity and obesity-related conditions, rare diseases, inflammatory conditions and cancer. As a member of the Amgen team, youll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.

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

**SENIOR MANAGER PROJECT CONTROLS**

**What you will do**

Lets do this. Lets change the world. In this vital role you will be accountable for managing, forecasting, and tracking costs, schedules, estimates and risks on a portfolio of capital projects at Amgens site located in New Albany, Ohio. This position is also partnered with all internal cross functional groups that support capital projects, including Engineering Technical Authority, Project Management, Facilities Management, Global Site Engineering, Capital Finance, and various Amgen internal business partners. The candidate should have the experience and ability to develop, train, and manage a team of cost managers and schedulers through partnership with our outside service providers.

**Role Location:**

The Project Controls Senior Manager is required to be local and work onsite at Amgens site in New Albany, Ohio.

- The Project Controls Senior Manager will be responsible for the following to support multiple, projects within their specific portfolio in key business areas: -
- Managing project controls from funding through close out, including compliance to processes and policies.
- Assisting Project Controls Director in developing project strategies and associated financing
- Working closely with the Front-End Planning team to develop conceptual estimates and schedules.
- Developing strategies and negotiating pricing for subcontractor scopes of work, reviewing, and analyzing engineer/contractor bids with GSS
- Monitoring and evaluating engineering and contractors physical progress.
- Addressing progress and delay claims from contractors
- Analysis and accurate review of engineering / construction cost forecasts against scope
- Reviewing and approving engineer and contractor buy outs, change orders and invoices.
- Preparing monthly cost reports and project status reports for senior management both on site and corporately.
- Lead the development, monitoring and reporting of project schedules and cash flow to enable accurate capital LE predication for their portfolio.
- Leading risk analysis reviews for cost estimates, forecasts and schedules using applicable software packages.
- Working with Amgen Buying Centre and Accounts Payable to resolve invoice payment issues and queries.
- Overseeing the closeout of contracts, purchase orders and subsequent projects within their portfolio.
- Monitoring and managing Capitalized Overhead across all projects and sites including planning, hiring, and charging processes.
- Exhibiting proactive safety leadership and behavior
- Communicating on and escalating on project matters and/or project controls performance for their portfolio to Site Sponsors and Engineering leadership
- Overseeing their portfolios project controls effectiveness and compliance utilizing strong analytical views to lead the project teams to ensure proper evaluation and analysis.
- Supporting Engineering Digital Transformation activities/workstreams by providing project controls subject matter expertise

**What we expect of you**

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

**Basic Qualifications:**

- High school diploma / GED and 12 years of Engineering and capital projects delivery
- experience OR
- Associates degree and 10 years of Engineering and capital projects delivery
- experience OR
- Bachelors degree and 6 years of Engineering and capital projects delivery experience OR
- Masters degree and 4 years of Engineering and capital projects delivery experience OR
- Doctorate degree and 2 years of Engineering and capital projects delivery experience

**Preferred Qualifications:**

- Experience in capital project delivery. managing Engineering or Construction in project controls across estimating, cost control, scheduling, and compliance

- 8 or more years within engineering or construction experience in the life sciences pharmaceutical/biotechnology industry executing project controls on projects (Funding, Estimating, Cost Management, Scheduling, Compliance, Contract Strategy)
- Strong analytic and problem-solving ability
- Excellent organizational and task management skills
- Effective communication skills and ability to translate / communicate details summarized to a variety of audiences.
- Ability to operate in a matrixed or team environment with site, functional, and executive leadership.
- Demonstrated ability to lead teams and build strong relationships across the network.
- Expertise and knowledge leading project controls internally and across external vendors
- Understanding the business aspects of projects to provide solutions to problems that require ingenuity and creativity.
- Experience in progress measurement methods such as Earned Value Management
- Experience in cost and scheduling software packages and data mining programs such as Power Bi
- Understanding workflows and dimensions of BIM and opportunities for integration with cost and schedule when managing capital projects
- Experience of procurement methods and contracts

**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 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. We make all employment decisions without regard to race, color, religion, sex or any other characteristic protected by applicable law.

We provide reasonable accommodations to applicants and employees with disabilities, consistent with legal requirements. Please contact us to request accommodation.

Engineer II

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.

**Engineer II**

Duties: Support the Corporate Environmental Sustainability program by developing, tracking, and reporting energy, carbon, water, and waste reduction metrics across global sites, with primary focus on refrigeration and cold room systems; Provide sustainability and environmental performance support for refrigeration and cold room projects, including CO (R744), ammonia, and other low-GWP systems within GMP-regulated environments; Assist with technical reviews of refrigeration and cold room project documentation including specifications, load calculations, controls, and performance data to support energy efficiency and sustainability goals, under the guidance of senior engineers or subject matter expert; Support refrigerant transition and decarbonization efforts by collecting asset inventories, operational data, and emissions inputs for existing refrigeration systems, and documenting findings for evaluation by senior engineering staff; Support analysis of refrigeration systemspecific energy and operational data using established methodologies to assist senior staff in evaluating potential energy-efficiency and emissions reduction opportunities; 6. Support alignment of refrigeration and cold room projects with environmental regulations, refrigerant standards including Environmental Protection Agency, American Society of Heating, Refrigerating and Air-Conditioning Engineers, and International Organization for Standardization, and corporate sustainability frameworks, ensuring technical compliance across global sites; Collaborate with engineering, facilities, quality, and sustainability teams to coordinate data, documentation, and sustainability deliverables associated with refrigeration projects; Maintain technical awareness of emerging refrigeration sustainability standards, regulatory changes, and industry best practices, including natural refrigerants and advancements in energy-efficient cold chain technologies; Assist in preparing sustainability documentation, analyses, reports, and preliminary assessments, including energy, emissions, cost-impact, water, and waste reduction opportunities using established templates; Support measurement and verification activities and benchmarking in accordance with established M&V protocols; Support coordination and participation in external sustainability initiatives, including the MIT CEP Energy Prize sponsorship and the BioPhorum Sustainability Water Workstream, by assisting with documentation, communications, and material preparation in alignment with corporate sustainability objectives; Assist with data compilation, documentation, and coordination activities related to ENERGY STAR award submissions and other sustainability recognition programs, including support for third-party audit processes; and Support development and implementation of electric vehicle (EV) infrastructure initiatives at existing sites by assisting with data analysis, documentation, and coordination activities. May telecommute.

Requirements: Masters degree (or foreign equivalent) in Chemical and Biomolecular Engineering or related field & 1 year of experience in the job offered or in an engineering-related occupation. Position requires 1 year of experience in the following:

- Supporting sustainability, energy efficiency, or environmental engineering projects within GMP-regulated biotech manufacturing environments;

- Applying measurement & verification principles to collect, calculate, and report energy performance data and support savings verification activities;

- Supporting conservation-focused or sustainability improvement projects under the direction of senior staff;

- Supporting water reduction initiatives by applying quantitative water balance analyses to calculate and document estimated water savings and water efficiency improvement opportunities for industrial or GMP-regulated manufacturing systems, including Purified Water (PW) and Water for Injection (WFI);

- Working on industrial refrigeration systems, including industrial-scale CO (R744) and other low-GWP refrigerants;

- Supporting sustainability reporting activities and environmental performance metrics calculations, including data preparation for Environmental, Social, and Governance and Carbon Disclosure Project reporting, using defined tools and templates;

- Supporting calculation of scope 1 and scope 2 emissions estimates for refrigeration systems; \\Supporting third-party energy performance validation programs or audits, including data collection and documentation for recognition programs such as ENERGY STAR;

- Supporting financial justification analyses including: Net Present Value, Rate of Return, and Simple Payback for sustainability initiatives;

- Enterprise ChatGPT modelling for business and engineering analysis; and

- PI Enterprise to extract and analyze energy, water, and operational data to support sustainability and performance assessments.

Measurement & Verification Professional (CMVP-IT or CMVP) certification required.

Contact: Interested candidates please apply via [https://careers.amgen.com/en/search-jobs](<https://careers.amgen.com/en/search-jobs>) and search for job # R-255472.

Job type: Full-Time position. The annual salary range for this position in the U.S. is $97,109.00 - $131,383.00 per year. Also, this position offers stock, retirement, medical, life and disability insurance and eligibility for an annual bonus or for sales roles, other incentive compensation. For more details visit[https://careers.amgen.com/life-at-amgen/benefits/](<https://urldefense.proofpoint.com/v2/url?u=https-3A__nam11.safelinks.protection.outlook.com_-3Furl-3Dhttps-253A-252F-252Furldefense.proofpoint.com-252Fv2-252Furl-253Fu-253Dhttps-2D3A-5F-5Fnam11.safelinks.protection.outlook.com-5F-2D3Furl-2D3Dhttps-2D253A-2D252F-2D252Furldefense.proofpoint.com-2D252Fv2-2D252Furl-2D253Fu-2D253Dhttps-2D2D3A-2D5F-2D5Fnam11.safelinks.protection.outlook.com-2D5F-2D2D3Furl-2D2D3Dhttps-2D2D253A-2D2D252F-2D2D252Furldefense.proofpoint.com-2D2D252Fv2-2D2D252Furl-2D2D253Fu-2D2D253Dhttps-2D2D2D3A-2D2D5F-2D2D5Fnam11.safelinks.protection.outlook.com-2D2D5F-2D2D2D3Furl-2D2D2D3Dhttps-2D2D2D253A-2D2D2D252F-2D2D2D252Furldefense.proofpoint.com-2D2D2D252Fv2-2D2D2D252Furl-2D2D2D253Fu-2D2D2D253Dhttps-2D2D2D2D3A-2D2D2D5F-2D2D2D5Fcareers.amgen.com-2D2D2D5Flife-2D2D2D2D2Dat-2D2D2D2D2Damgen-2D2D2D5Fbenefits-2D2D2D5F-2D2D2D2526d-2D2D2D253DDwMGaQ-2D2D2D2526c-2D2D2D253D6HFirGB4LnuU4asVt8kNcMhC5SvBtxbjoaC4-2D2D2D2DrMbhtk-2D2D2D2526r-2D2D2D253DZzsBV9k-2D2D2D2DjttVNN1EvZst0Q-2D2D2D2526m-2D2D2D253DbXelMAn-2D2D2D2DLkr6ITgl-2D2D2D2DOVIwCkmHKYirp3gc83wvPae1SgtYIJYqwI2avmaKPLstizO-2D2D2D2526s-2D2D2D253DkeznBgK-2D2D2D2DF4tRtUWSI5ABybrJF1hszDEySq52Jge-2D2D2D2D2Mk-2D2D2D2526e-2D2D2D253D-2D2D2D26data-2D2D2D3D05-2D2D2D257C01-2D2D2D257Cjen01-2D2D2D2540amgen.com-2D2D2D257C660a28539c1044de1e4108db272cafda-2D2D2D257C4b4266a6136841afad5a59eb634f7ad8-2D2D2D257C0-2D2D2D257C0-2D2D2D257C638146845207554495-2D2D2D257CUnknown-2D2D2D257CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0-2D2D2D253D-2D2D2D257C3000-2D2D2D257C-2D2D2D257C-2D2D2D257C-2D2D2D26sdata-2D2D2D3DcYzBM3rFPl6qL6wF1v5QiaiQBXGj4x6xspFO9HqU9Vg-2D2D2D253D-2D2D2D26reserved-2D2D2D3D0-2D2D2526d-2D2D253DDwMGaQ-2D2D2526c-2D2D253D6HFirGB4LnuU4asVt8kNcMhC5SvBtxbjoaC4-2D2D2DrMbhtk-2D2D2526r-2D2D253DZzsBV9k-2D2D2DjttVNN1EvZst0Q-2D2D2526m-2D2D253DUnLMPhr-2D2D2DEGnpr9XBuHlwWv-2D2D2Dn4T7T8VuRZFDjwpT9dOvwdZKz7drSop9P1WDp591w-2D2D2526s-2D2D253Dc0sqSn-2D2D2DN3CobCiFz89Y-2D2D2Ds8tVcO-2D2D2D8OnDdCGlXU0NbgBc-2D2D2526e-2D2D253D-2D2D26data-2D2D3D05-2D2D257C01-2D2D257Crodneyj-2D2D2540amgen.com-2D2D257>)

What you can expect of us

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

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

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

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

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

- Stock-based long-term incentives

- Award-winning time-off plans

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

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

careers.amgen.com

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

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.

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.

Engineer - Physical Methods

**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. Amgen is advancing a broad and deep pipeline and portfolio of medicines to treat heart disease, obesity and obesity-related conditions, rare diseases, inflammatory conditions and cancer. 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.

**Engineer**

**What you will do**

Lets do this. Lets change the world. In this vital role you will be responsible for engineering activities required for the development, qualification, validation, transfer and life cycle management of physical GMP test methods for combination products, devices, primary containers, and secondary packaging components. The Engineer shall have the ability to work on multiple projects at the same time. The work involves design and development of test methods for measuring physical attributed like dimension, force, time, , and/or for qualitative inspection of components (e.g., visual inspection for defect). It includes ideation of test concept, tooling and prototyping fixtures, proof of concept, feasibility and robustness, qualification of test equipment, evaluation of method characteristics, validation and transfer of the test method. It would be for new products, processes, tooling or equipment introduction to improve quality and reliability and reduce costs.

- Develop, qualify, validate GMP physical test methods for vials, prefilled syringes, and injection devices.
- Work in teams to transfer new combination product test method and assembly requirements to manufacturing, by developing six sigma processes and compiling documentation for manufacturing assembly requirements.
- Develop, qualify, validate, and transfer new equipment, software, systems, and methods.
- Implement projects per Combination Product Organization (CPO) and company procedures to ensure projects are completed on schedule and within established budget.
- Provide expert support for investigations as well as new process development required to improve manufacturing operations.
- Coordinate test method development and delivery with selected contractors.
- Ensure that qualification parameters are met for product assembly requirements.
- Support development of cost estimates for new processes, gauges and equipment development used in generation of capital request documentation.
- Generate procedures necessary to support department and new process equipment.
- Provide expert training to individuals in the operation and maintenance of processes, test methods and equipment introduced to Quality Control and/or the manufacturing department (i.e. production operator, mechanics, process engineers).
- Participate in and assume responsibilities of team functions as assigned (i.e. Product Improvement Teams).
- Generate/author and own the Test Method documents.
- Gather test method requirements that result in equipment that operates safely and considers ergonomic factors in the design
- Perform other duties as required by the Group Manager
- Follow the requirements, responsibilities, and authority as required
- Maintains integrated timelines capturing appropriate cross functional details and deliverables which are aligned with the functional and project deliverables
- Networks internally to ensure alignment, commitment to project objectives and timelines as well as to ensure effective execution of projects
- Networks with manufacturing, quality and regulatory organizations both internal and external to Amgen
- Drives the cross-functional communication and integration of information to optimize decision making, issue resolution and change management throughout project lifecycle
- Excellent verbal and written communication skills are applied to communicate project status and risks associated with integrated timelines to leadership
- Collaborates with other functional leaders to ensure project success, momentum and commitment
- Proactively identifies issues and/or risks and develops mitigation options to resolve or escalate efficiently
- Integrates partner/vendor timelines with Amgen timelines as appropriate
- Assist with CAPAs and change controls for the continuous improvement and lifecycle management of production transferred methods
- The position will require approximately 10% travel (including international locations)

**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 go getter with these qualifications.

**Basic Qualifications:**

Masters degree

OR

Bachelors degree and 2 years of **Engineering** experience

OR

Associates degree and 6 years of **Engineering**

OR

High school diploma / GED and 8 years of **Engineering** experience

**Preferred Qualifications:**

- M.S. (Or Doctoral) degree in Mechanical Engineer, Biomedical Engineering or closely related fields.
- Excellent written and verbal communication skills
- Ability to work in a highly matrixed team environment
- 2 years of experience in the biotechnology/pharmaceutical industry
- 2 years of experience in equipment, method, and mechanical design
- Technical writing experience
- Experience with SolidWorks (or other 3D-CAD software)
- Experience with combination products and regulatory requirements
- Experience using Minitab (or other statistical software packages)
- Experience with machine controls (PLC, HMI) and vision systems

**What you can expect of us**

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

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 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. We make all employment decisions without regard to race, color, religion, sex or any other characteristic protected by applicable law.

We provide reasonable accommodations to applicants and employees with disabilities, consistent with legal requirements. Please contact us to request accommodation.

United States Pharmacopeia

Associate Software Engineer

**Description**

**Who is USP?**

The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world’s leading health and science experts to develop rigorous quality standards for medicines, dietary supplements, and food ingredients. At USP, we believe that scientific excellence is driven by a commitment to fairness, integrity, and global collaboration. This belief is embedded in our core value of Passion for Quality and is demonstrated through the contributions of more than 1,300 professionals across twenty global locations, working to strengthen the supply of safe, high-quality medicines worldwide.

At USP, we value inclusive scientific collaboration and recognize that attracting diverse expertise strengthens our ability to develop trusted public health standards. We foster an organizational culture that supports equitable access to mentorship, professional development, and leadership opportunities. Our partnerships, standards, and research reflect our belief that ensuring broad participation in scientific leadership results in stronger, more impactful outcomes for global health.

USP is proud to be an equal employment opportunity employer (EEOE) and is committed to ensuring fair, merit-based selection processes that enable the best scientific minds—regardless of background—to contribute to advancing public health solutions worldwide. We provide reasonable accommodations to individuals with disabilities and uphold policies that create an inclusive and collaborative work environment.

**Brief Job Overview**

The Associate Software Engineer – is responsible for supporting and enhancing the Marketo platform through technical configuration, integration management, campaign automation, and data governance. This role partners with IT, Marketing Operations, and Sales Operations to ensure scalable, reliable, and compliant marketing automation processes. The engineer owns day‑to‑day platform operations while contributing to system improvements and cross‑system alignment.

**How will YOU create impact here at USP?**

As part of our mission to advance scientific rigor and public health standards, you will play a vital role in increasing global access to high-quality medicines through public standards and related programs. USP prioritizes scientific integrity, regulatory excellence, and evidence-based decision-making to ensure health systems worldwide can rely on strong, tested, and globally relevant quality standards.

Additionally, USP’s People and Culture division, in partnership with the Equity Office, invests in leadership and workforce development to equip all employees with the skills to create high-performing, inclusive teams. This includes training in equitable management practices and tools to promote engaged, collaborative, and results-driven work environments.

**The Associate Software Engineer** **has the following responsibilities:**

- Support user account creation, access permissions, and role governance across marketing automation and CRM platforms to maintain secure, compliant operations.
- Translate stakeholder requirements into technical configurations, reusable templates, and scalable operational solutions within a marketing automation platform (e.g., Marketo, HubSpot, Pardot, or similar).
- Help maintain platform architecture — folder structures, naming conventions, tokens, and operational program frameworks.
- Build and maintain field mappings and synchronization logic between the marketing platform and CRM (e.g., Salesforce), supporting schema alignment and data quality.
- Clone, configure, and test forms, landing pages, and web assets in Sandbox and Production environments using HTML/CSS fundamentals.
- Troubleshoot sync issues between systems, including field conflicts, validation errors, and API-related failures — with support from senior engineers as needed.
- Assist with datatype changes, schema updates, and cross-system compatibility checks to keep integrations stable.
- Support Sandbox refresh activities: configuration audits, asset restoration, and sync re-establishment.
- Help build and maintain trigger-based campaigns, automated workflows, and nurture programs, learning platform-specific logic on the job.
- Assist with segmentation setup, audience management, and basic data governance practices.
- Monitor system health and campaign performance dashboards, flagging issues to senior team members.
- Support data quality and compliance standards across marketing and CRM systems.

**Who is USP Looking For?**

The successful candidate will have a demonstrated understanding of our mission, commitment to excellence through inclusive and equitable behaviors and practices, ability to quickly build credibility with stakeholders, along with the following competencies and experience:

- Bachelor's degree in Computer Science, Information Systems, Engineering, or a related technical field (or equivalent practical experience).
- 1–2 years of experience in a technical, engineering, or systems support role.
- Working knowledge of HTML and CSS; exposure to basic JavaScript is a plus.
- Understanding of how APIs and webhooks work, or strong aptitude to learn integration concepts quickly.
- Interest in or exposure to CRM systems (Salesforce, HubSpot, etc.) and/or marketing automation platforms — prior hands-on Marketo experience is **not required** .
- Comfort working with structured data: field mapping, data types, and schema logic.
- Strong problem-solving instincts and willingness to troubleshoot systematically.
- Clear communicator, able to explain technical issues to both technical and non-technical stakeholders.

**Additional Desired Preferences**

- Any exposure to Marketo, HubSpot, Pardot, or similar marketing automation tools.
- Familiarity with CRM objects (Leads/Contacts/Accounts/Opportunities).
- Coursework or personal projects involving REST APIs or third-party integrations (e.g., ad platforms like Google, Meta, or LinkedIn).
- Certifications are a plus but not expected at this level (e.g., Marketo Certified Associate/Expert, Salesforce Admin).

**Supervisory Responsibilities**

None, this is an individual contributor role.

**Benefits**

USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected.

**Compensation**

Base Salary Range: **USD $71,420.00 – $93,726.00 annually** .

Target Annual Bonus: % Varies based on level of role.

Individual compensation packages are based on various factors unique to each candidate’s skill set, experience, qualifications, equity, and other job-related reasons.

Note: USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP.

Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities

This employer is required to notify all applicants of their rights pursuant to federal employment laws.

For further information, please review the Know Your Rights (https://www.eeoc.gov/poster) notice from the Department of Labor.

**Job Category** Information Technology

**Job Type** Full-Time

Maryland

Sanofi US

Plant Process Commissioning Qualification Engineer

**Job Title**: Plant Process Commissioning Qualification Engineer

- Location: Swiftwater, PA

**About the Job**

The Plant Process Commissioning Qualification Engineer is a critical engineering quality review and execution support role responsible for the consistent application governance and maintenance of Commissioning and Qualification Engineering platform procedures In this role you will apply Commissioning and Qualification testing templates engineering standards and specifications across both OPEX and CAPEX projects You will directly support antigen and filling manufacturing operations with a strong emphasis on Inspection and Packaging processes work that ultimately protects patients and ensures the integrity of life saving vaccines and pharmaceutical products.

Join a global network that powers how Sanofi delivers seamlessly, purposefully, and at scale. In Manufacturing & Supply, youll help reimagine how life-changing treatments reach people everywhere, faster.

**About Sanofi:**

Were an R&D-driven, AI-powered biopharma company committed to improving peoples lives and delivering compelling growth. Our deep understanding of the immune system and innovative pipeline enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve lives.

**Main Responsibilities**

- Review and approval of SAT FAT Commissioning and Qualification and Design documentation protocols test scripts reports assessments.
- Impact assessments Change Control Functional Component and Design Review Design Qualification DRDQ.
- Protocol and Test Script authoring.
- Continuous improvement authoring updates to site Commissioning and Qualification platform procedures
- Engineering Change Management process
- Contractor management

This role offers a dynamic blend of technical leadership quality governance and cross functional collaboration.

**As a key member of our engineering team, you will**

- Serve as the primary Commissioning and Qualification Engineering interface with project management and project controls functions supporting contractor budget and schedule performance measurements and reporting Provide strong Commissioning and Qualification focus and oversight for packaging and inspection systems.
- Provide Commissioning and Qualification support for projects focusing equipment and utilities to support Drug substance processing Final Filling process and Inspection and Packaging
- Review and approve protocols test scripts data packs and reports to ensure consistent high-quality engineering documentation across all assigned projects.
- Audit engineering quality in accordance with site and project level Commissioning and Qualification plans development qualification Global Engineering Guidelines and Quality Operational Qualification Guidelines.
  Update and approve site Commissioning and Qualification platform methods and procedures ensuring alignment with project lessons learned GEG updates and global quality document revisions.
- Support technical engineering staff in the use and documentation of the engineering change management process.
- Execute audit initiatives and remediation activities including action items resulting from internal and external audits change controls and deviation remediation as directed by the Plant Process and Commissioning and Qualification Lead and or Site Project Engineering Lead
- Manage contract associates as required to support Commissioning and Qualification activities.

**Scope and Impact**

Your work will directly influence the quality and compliance of engineering documentation across both CAPEX and OPEX projects by applying Global Engineering Guidelines and local engineering methods you will ensure that every project meets the highest standards of engineering and regulatory excellence Specific activities include

- Executing System and Functional Component Criticality Assessments
- Conducting Design Review and Qualification activities
- Authoring Protocols Test Scripts and Reports as assigned
- Authoring technical assessments in support of change controls deviations and CAPA

**About You**

**Basic qualifications**

- Bachelors degree in Engineering, Pharmaceutical Sciences, Life Sciences, Biotechnology, Computer sciences or other related technical fields.
- 5+ years of experience in Commissioning, Qualification, Testing Equipment, quality assurance, Engineering, Packaging or other related fields.

**Additional skills:**

- Packaging and Inspection process systems
- Process Equipment Filling systems isolators purification systems
- Chromatography systems autoclaves washers and Controlled Temperature Units
- GMP Utilities WFI Clean Steam Clean Compressed Air
- Experience in the vaccine or pharmaceutical industry
- Demonstrated expertise in the quality review of good documentation practices
- GDP Knowledge of quality and regulatory requirements applicable to pharmaceutical and biotech manufacturing
- Experience with contemporary commissioning and qualification methods

**Why choose us?**

- Bring the miracles of science to life alongside a supportive, future-focused team.
- Discover endless opportunities to grow your talent and drive your career, whether its through a promotion or lateral move, at home or internationally.
- Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
- Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention andwellness programs and at least 14 weeks gender-neutral parental leave.
- Shape the future of medicine and vaccine delivery with cutting-edge technology, ensuring seamless launches and a resilient global supply.
- Power industry-leading performance by leveraging digital, data, and AI-driven innovation at speed and scale
- Transform lives worldwide by delivering life-changing treatments anywhere, anytime.

Sanofi Inc. and its U.S. affiliates are Equal Opportunity employers committed to a culturally inclusive workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.

\#GD-SP

\#LI-SP

\#VHD

All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can [be found here.](<https://benefits.sanofiusallwell.com/fleet/public/index/ba511bf8-5c32-4828-9861-ab985fffab90/?cid=sanofi>)

Pennsylvania

Specialist Software Engineer

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.

**Specialist Software Engineer**

Duties: Software application Dev/Ops on Amgens Salesforce.com platform using Apex, Visual Force, and Lightning Web Components for Service, B2B Commerce and experience cloud capabilities; Develop and maintain customizations for solutions delivery utilizing Salesforce Service, Commerce, Experience Cloud platforms which are a customer service platforms designed to help organizations deliver superior customer support and improve customer satisfaction; Work on MuleSoft integration platform to help businesses connect applications and services; Use DocuSign and Conga platforms to securely sign, send, and manage documents online; Configure and model the Salesforce.com application based on the business requirements; Build Service cloud capabilitiessetup accounts & contracts, cases, email-to-case and omni channel rules targeting business requirements; Build B2B Commerce cloud capabilitiesset up products, orders, carts, entitlements, order status standard and custom objects per business requirements; Lead the technical configuration of standard and custom objects developed, experience cloud portal, and API customization; Formulate sound technical solutions to common Order to Cash cycle, Distribution & Logistics business requirements; and Communicate software and system designs using UML, lucid chart or other modeling tools and software. May telecommute.

Requirements: Masters degree (or foreign equivalent) in Computer Science, Software Engineering or related field & 3 years of experience in the job offered or a software-related occupation. Position requires 3 years of experience in the following:

- Apex, Visualforce, and Lightning Web Components for Service Cloud, B2B Commerce, and Experience Cloud capabilities;

- Apex, SOQL, Lightning Web Components, JavaScript, Visualforce, AJAX, HTML, XML, CSS, Process Builder, Flow Management, Custom Settings, Workflow Rules, Triggers, Data Loader, Reports, Dashboards, REST APIs, and SOAP Web Services;

- Salesforce Experience Cloud (Communities) including development of customer and partner portals using Experience Builder, Lightning Web Components, Apex, Visualforce, CMS, custom components, and security and sharing configurations;

- Service Cloud capabilities including Case Management, Email-to-Case, Omni-Channel, Knowledge Base, and Reporting and Analytics;

- Scalable data processing solutions in Salesforce including Batch Apex, Scheduled Apex, Queueable Apex, and asynchronous processing mechanisms;

- Managing Salesforce release and deployment processes including change set management, deployment validation, environment management, and version control using Copado and related DevOps tools;

- Salesforce migration and deployment tools including Copado, ANT Migration Tool, Salesforce CLI (SFDX), and CI/CD pipelines to support code promotion across environments;

- SAFe Agile practices including PI Planning, Sprint Planning, Backlog Management, and Agile ceremonies using project management tools such as Jira and Confluence;

- Supply chain processes including Order-to-Cash, Global Distribution, Customer Service, and Logistics; and

- Web services, data modeling, and enterprise application integration concepts, including implementing Salesforce integrations with MuleSoft, Conga, and DocuSign.

Contact: Interested candidates please apply via [https://careers.amgen.com/en/search-jobs](<https://careers.amgen.com/en/search-jobs>) and search for job # R-255470.

Job type: Full-Time position. The annual salary for this position in the U.S. is $173,659.00 per year. Also, this position offers stock, retirement, medical, life and disability insurance and eligibility for an annual bonus or for sales roles, other incentive compensation. For more details visit[https://careers.amgen.com/life-at-amgen/benefits/](<https://urldefense.proofpoint.com/v2/url?u=https-3A__nam11.safelinks.protection.outlook.com_-3Furl-3Dhttps-253A-252F-252Furldefense.proofpoint.com-252Fv2-252Furl-253Fu-253Dhttps-2D3A-5F-5Fnam11.safelinks.protection.outlook.com-5F-2D3Furl-2D3Dhttps-2D253A-2D252F-2D252Furldefense.proofpoint.com-2D252Fv2-2D252Furl-2D253Fu-2D253Dhttps-2D2D3A-2D5F-2D5Fnam11.safelinks.protection.outlook.com-2D5F-2D2D3Furl-2D2D3Dhttps-2D2D253A-2D2D252F-2D2D252Furldefense.proofpoint.com-2D2D252Fv2-2D2D252Furl-2D2D253Fu-2D2D253Dhttps-2D2D2D3A-2D2D5F-2D2D5Fnam11.safelinks.protection.outlook.com-2D2D5F-2D2D2D3Furl-2D2D2D3Dhttps-2D2D2D253A-2D2D2D252F-2D2D2D252Furldefense.proofpoint.com-2D2D2D252Fv2-2D2D2D252Furl-2D2D2D253Fu-2D2D2D253Dhttps-2D2D2D2D3A-2D2D2D5F-2D2D2D5Fcareers.amgen.com-2D2D2D5Flife-2D2D2D2D2Dat-2D2D2D2D2Damgen-2D2D2D5Fbenefits-2D2D2D5F-2D2D2D2526d-2D2D2D253DDwMGaQ-2D2D2D2526c-2D2D2D253D6HFirGB4LnuU4asVt8kNcMhC5SvBtxbjoaC4-2D2D2D2DrMbhtk-2D2D2D2526r-2D2D2D253DZzsBV9k-2D2D2D2DjttVNN1EvZst0Q-2D2D2D2526m-2D2D2D253DbXelMAn-2D2D2D2DLkr6ITgl-2D2D2D2DOVIwCkmHKYirp3gc83wvPae1SgtYIJYqwI2avmaKPLstizO-2D2D2D2526s-2D2D2D253DkeznBgK-2D2D2D2DF4tRtUWSI5ABybrJF1hszDEySq52Jge-2D2D2D2D2Mk-2D2D2D2526e-2D2D2D253D-2D2D2D26data-2D2D2D3D05-2D2D2D257C01-2D2D2D257Cjen01-2D2D2D2540amgen.com-2D2D2D257C660a28539c1044de1e4108db272cafda-2D2D2D257C4b4266a6136841afad5a59eb634f7ad8-2D2D2D257C0-2D2D2D257C0-2D2D2D257C638146845207554495-2D2D2D257CUnknown-2D2D2D257CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0-2D2D2D253D-2D2D2D257C3000-2D2D2D257C-2D2D2D257C-2D2D2D257C-2D2D2D26sdata-2D2D2D3DcYzBM3rFPl6qL6wF1v5QiaiQBXGj4x6xspFO9HqU9Vg-2D2D2D253D-2D2D2D26reserved-2D2D2D3D0-2D2D2526d-2D2D253DDwMGaQ-2D2D2526c-2D2D253D6HFirGB4LnuU4asVt8kNcMhC5SvBtxbjoaC4-2D2D2DrMbhtk-2D2D2526r-2D2D253DZzsBV9k-2D2D2DjttVNN1EvZst0Q-2D2D2526m-2D2D253DUnLMPhr-2D2D2DEGnpr9XBuHlwWv-2D2D2Dn4T7T8VuRZFDjwpT9dOvwdZKz7drSop9P1WDp591w-2D2D2526s-2D2D253Dc0sqSn-2D2D2DN3CobCiFz89Y-2D2D2Ds8tVcO-2D2D2D8OnDdCGlXU0NbgBc-2D2D2526e-2D2D253D-2D2D26data-2D2D3D05-2D2D257C01-2D2D257Crodneyj-2D2D2540amgen.com-2D2D257>)

What you can expect of us

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

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

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

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

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

- Stock-based long-term incentives

- Award-winning time-off plans

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

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

careers.amgen.com

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

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.

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 Associate

Join Amgens Mission of Serving Patients

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

Since 1980, weve helped pioneer the world of biotech in our fight against the worlds toughest diseases. With our focus on four therapeutic areas Oncology, Inflammation, General Medicine, and Rare Disease we reach millions of patients each year. 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 Associate**

Duties: Perform method development and qualification studies using High Performance Liquid Chromatography (HPLC), Ultra-High Performance Liquid Chromatography (UHPLC), and Capillary Electrophoresis (CE) platforms; Perform chromatographic fractionation, peptide mapping, intact mass, and other Liquid Chromatography Mass Spectrometry (LC-MS) studies to support product characterization and comparability studies; Author results in laboratory notebooks and method development reports, interfacing closely with Attribute Sciences Team Leads and Quality Control to transfer and troubleshoot qualified methods; Participate in the maintenance of Attribute Sciences instruments and assist the Attribute Sciences department in maintaining a phase-appropriate good manufacturing practices (GMP) environment; Focus toward evaluation of critical quality attributes, coordinate and perform attribute identification and characterization studies, including isolation and analysis of chromatography fractions; Conduct and coordinate accelerated stability studies to define therapeutic degradative pathways; Perform evaluation of novel platform analytical technologies to help drive innovation; and Perform experiments to help answer questions from health authorities; and Collaborate with partner organizations during commercial process development, process characterization, and process validation studies to support marketing applications.

Requirements: Bachelors degree (or foreign equivalent) in Chemistry, Chemical Biology or related field & 2 years of experience in the job offered or a research-related occupation. Position requires 2 years of experience in the following:

- Analytical chemistry experience for protein molecules, and completion of project deliverables including: designing and conducting degradation experiments, extracting and analyzing results via dedicated software: Empower, Chromeleon, and ChemStation;

- Liquid Chromatography principles, including the concepts of stationary and mobile phases, partitioning and separation based on different affinities;

- Analytical method development (chromatography and mass spectrometry), technologies and instrumentation including: High Performance Liquid Chromatography (HPLC), Liquid Chromatography Mass Spectrometry (LC-MS), Solo Variable Pathlength Extension (SoloVPE), and Capillary Electrophoresis (CE);

- Method qualification and transfer for analytical instruments, along with data analysis and statistical evaluation of experimental results;

- Application analytical instrument troubleshooting across different platforms: Waters, Agilent, and Maurice;

- Analytical deliverables for pharmaceutical processes and product development;

- Data analysis, statistical analysis and method qualifications and transfers;

- Technical knowledge of proteins and peptides;

- Implementing Standard Operating Procedures in a laboratory environment in accordance with good laboratory practices (GLP) standards; and

- Recording experimental conditions, results and observations in a laboratory notebook.

Contact: Interested candidates please apply via [https://careers.amgen.com/en/search-jobs](<https://careers.amgen.com/en/search-jobs>) and search for job # R-255469.

Job type: Full-Time position. The annual salary range for this position in the U.S. is $91,125.00 - $108,296.00 per year. Also, this position offers stock, retirement, medical, life and disability insurance and eligibility for an annual bonus or for sales roles, other incentive compensation. For more details visit[https://careers.amgen.com/life-at-amgen/benefits/](<https://urldefense.proofpoint.com/v2/url?u=https-3A__nam11.safelinks.protection.outlook.com_-3Furl-3Dhttps-253A-252F-252Furldefense.proofpoint.com-252Fv2-252Furl-253Fu-253Dhttps-2D3A-5F-5Fnam11.safelinks.protection.outlook.com-5F-2D3Furl-2D3Dhttps-2D253A-2D252F-2D252Furldefense.proofpoint.com-2D252Fv2-2D252Furl-2D253Fu-2D253Dhttps-2D2D3A-2D5F-2D5Fnam11.safelinks.protection.outlook.com-2D5F-2D2D3Furl-2D2D3Dhttps-2D2D253A-2D2D252F-2D2D252Furldefense.proofpoint.com-2D2D252Fv2-2D2D252Furl-2D2D253Fu-2D2D253Dhttps-2D2D2D3A-2D2D5F-2D2D5Fnam11.safelinks.protection.outlook.com-2D2D5F-2D2D2D3Furl-2D2D2D3Dhttps-2D2D2D253A-2D2D2D252F-2D2D2D252Furldefense.proofpoint.com-2D2D2D252Fv2-2D2D2D252Furl-2D2D2D253Fu-2D2D2D253Dhttps-2D2D2D2D3A-2D2D2D5F-2D2D2D5Fcareers.amgen.com-2D2D2D5Flife-2D2D2D2D2Dat-2D2D2D2D2Damgen-2D2D2D5Fbenefits-2D2D2D5F-2D2D2D2526d-2D2D2D253DDwMGaQ-2D2D2D2526c-2D2D2D253D6HFirGB4LnuU4asVt8kNcMhC5SvBtxbjoaC4-2D2D2D2DrMbhtk-2D2D2D2526r-2D2D2D253DZzsBV9k-2D2D2D2DjttVNN1EvZst0Q-2D2D2D2526m-2D2D2D253DbXelMAn-2D2D2D2DLkr6ITgl-2D2D2D2DOVIwCkmHKYirp3gc83wvPae1SgtYIJYqwI2avmaKPLstizO-2D2D2D2526s-2D2D2D253DkeznBgK-2D2D2D2DF4tRtUWSI5ABybrJF1hszDEySq52Jge-2D2D2D2D2Mk-2D2D2D2526e-2D2D2D253D-2D2D2D26data-2D2D2D3D05-2D2D2D257C01-2D2D2D257Cjen01-2D2D2D2540amgen.com-2D2D2D257C660a28539c1044de1e4108db272cafda-2D2D2D257C4b4266a6136841afad5a59eb634f7ad8-2D2D2D257C0-2D2D2D257C0-2D2D2D257C638146845207554495-2D2D2D257CUnknown-2D2D2D257CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0-2D2D2D253D-2D2D2D257C3000-2D2D2D257C-2D2D2D257C-2D2D2D257C-2D2D2D26sdata-2D2D2D3DcYzBM3rFPl6qL6wF1v5QiaiQBXGj4x6xspFO9HqU9Vg-2D2D2D253D-2D2D2D26reserved-2D2D2D3D0-2D2D2526d-2D2D253DDwMGaQ-2D2D2526c-2D2D253D6HFirGB4LnuU4asVt8kNcMhC5SvBtxbjoaC4-2D2D2DrMbhtk-2D2D2526r-2D2D253DZzsBV9k-2D2D2DjttVNN1EvZst0Q-2D2D2526m-2D2D253DUnLMPhr-2D2D2DEGnpr9XBuHlwWv-2D2D2Dn4T7T8VuRZFDjwpT9dOvwdZKz7drSop9P1WDp591w-2D2D2526s-2D2D253Dc0sqSn-2D2D2DN3CobCiFz89Y-2D2D2Ds8tVcO-2D2D2D8OnDdCGlXU0NbgBc-2D2D2526e-2D2D253D-2D2D26data-2D2D3D05-2D2D257C01-2D2D257Crodneyj-2D2D2540amgen.com-2D2D257>)

What you can expect of us

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

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

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

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

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

- Stock-based long-term incentives

- Award-winning time-off plans

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

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

careers.amgen.com

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

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.

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.

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.

**Specialist Software Engineer**

Duties: Work in an agile team to mature platform capabilities though backlog grooming, sprint planning and other agile ceremonies; Provide guidance to cross-functional teams on the platform methods and best practices such as: application and integration development methodologies, architecture standards, functional and technical solutions, environment management, testing, and platform education; Solve key implementation issues and demonstrate ability to work towards successful resolution; Negotiate solutions to problems with both internal teams and third-party service providers; Build relationships and work with cross-functional teams and contribute to broader goals and growth beyond the scope of a single role; Drive architectural governance by conducting comprehensive code reviews of test automation solutions, ensuring compliance with quality standards and industry best practices. Lead the architecture and implementation of reusable test automation frameworks and accelerators to ensure scalable expansion of existing functionality; Accelerate test automation adoption through focused enablement initiatives and strategic engagement; and Drive the design and execution of the data deployment solution, establishing standards and ensuring operational excellence. May telecommute.

Requirements: Masters degree (or foreign equivalent) in Computer Science, Computer Engineering, Information Systems, or a related field & 2 years of experience the job offered or in a software-related occupation. Position requires 2 years of experience in the following:

- Implementing and leading Salesforce solutions;

- Copado DevOps, including pipeline design and deployment automations;

- Copado Robotic Testing (CRT) across designing, developing, and maintaining advanced automation suites and accelerators;

- Agile framework;

- Object-oriented programming principles with Apex ;

- Working with test management and defect tracking tools including Zephyr and ALM;

- Building or integrating automation reporting and analytics; and

- GenAI tools or intelligent test automation platforms.

Contact: Interested candidates please apply via [https://careers.amgen.com/en/search-jobs](<https://careers.amgen.com/en/search-jobs>) and search for job # R-255466.

Job type: Full-Time position. The annual salary range for this position in the U.S. is $126,570.00 - $171,242.00 per year. Also, this position offers stock, retirement, medical, life and disability insurance and eligibility for an annual bonus or for sales roles, other incentive compensation. For more details visit[https://careers.amgen.com/life-at-amgen/benefits/](<https://urldefense.proofpoint.com/v2/url?u=https-3A__nam11.safelinks.protection.outlook.com_-3Furl-3Dhttps-253A-252F-252Furldefense.proofpoint.com-252Fv2-252Furl-253Fu-253Dhttps-2D3A-5F-5Fnam11.safelinks.protection.outlook.com-5F-2D3Furl-2D3Dhttps-2D253A-2D252F-2D252Furldefense.proofpoint.com-2D252Fv2-2D252Furl-2D253Fu-2D253Dhttps-2D2D3A-2D5F-2D5Fnam11.safelinks.protection.outlook.com-2D5F-2D2D3Furl-2D2D3Dhttps-2D2D253A-2D2D252F-2D2D252Furldefense.proofpoint.com-2D2D252Fv2-2D2D252Furl-2D2D253Fu-2D2D253Dhttps-2D2D2D3A-2D2D5F-2D2D5Fnam11.safelinks.protection.outlook.com-2D2D5F-2D2D2D3Furl-2D2D2D3Dhttps-2D2D2D253A-2D2D2D252F-2D2D2D252Furldefense.proofpoint.com-2D2D2D252Fv2-2D2D2D252Furl-2D2D2D253Fu-2D2D2D253Dhttps-2D2D2D2D3A-2D2D2D5F-2D2D2D5Fcareers.amgen.com-2D2D2D5Flife-2D2D2D2D2Dat-2D2D2D2D2Damgen-2D2D2D5Fbenefits-2D2D2D5F-2D2D2D2526d-2D2D2D253DDwMGaQ-2D2D2D2526c-2D2D2D253D6HFirGB4LnuU4asVt8kNcMhC5SvBtxbjoaC4-2D2D2D2DrMbhtk-2D2D2D2526r-2D2D2D253DZzsBV9k-2D2D2D2DjttVNN1EvZst0Q-2D2D2D2526m-2D2D2D253DbXelMAn-2D2D2D2DLkr6ITgl-2D2D2D2DOVIwCkmHKYirp3gc83wvPae1SgtYIJYqwI2avmaKPLstizO-2D2D2D2526s-2D2D2D253DkeznBgK-2D2D2D2DF4tRtUWSI5ABybrJF1hszDEySq52Jge-2D2D2D2D2Mk-2D2D2D2526e-2D2D2D253D-2D2D2D26data-2D2D2D3D05-2D2D2D257C01-2D2D2D257Cjen01-2D2D2D2540amgen.com-2D2D2D257C660a28539c1044de1e4108db272cafda-2D2D2D257C4b4266a6136841afad5a59eb634f7ad8-2D2D2D257C0-2D2D2D257C0-2D2D2D257C638146845207554495-2D2D2D257CUnknown-2D2D2D257CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0-2D2D2D253D-2D2D2D257C3000-2D2D2D257C-2D2D2D257C-2D2D2D257C-2D2D2D26sdata-2D2D2D3DcYzBM3rFPl6qL6wF1v5QiaiQBXGj4x6xspFO9HqU9Vg-2D2D2D253D-2D2D2D26reserved-2D2D2D3D0-2D2D2526d-2D2D253DDwMGaQ-2D2D2526c-2D2D253D6HFirGB4LnuU4asVt8kNcMhC5SvBtxbjoaC4-2D2D2DrMbhtk-2D2D2526r-2D2D253DZzsBV9k-2D2D2DjttVNN1EvZst0Q-2D2D2526m-2D2D253DUnLMPhr-2D2D2DEGnpr9XBuHlwWv-2D2D2Dn4T7T8VuRZFDjwpT9dOvwdZKz7drSop9P1WDp591w-2D2D2526s-2D2D253Dc0sqSn-2D2D2DN3CobCiFz89Y-2D2D2Ds8tVcO-2D2D2D8OnDdCGlXU0NbgBc-2D2D2526e-2D2D253D-2D2D26data-2D2D3D05-2D2D257C01-2D2D257Crodneyj-2D2D2540amgen.com-2D2D257>)

What you can expect of us

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

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

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

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

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

- Stock-based long-term incentives

- Award-winning time-off plans

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

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

careers.amgen.com

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

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.

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 - CIP/SIP/Autoclaves

**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-CIP/SIP/Autoclave**

**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 onCIP, SIP and Autoclave engineering and plant equipment.

Demonstrate technical expertise and provide lifecycle support for CIP skid systems, SIP circuits, autoclaves, transfer panels, process tanks, valves, instrumentation, and associated automation platforms. The role will support commissioning, qualification, startup readiness, routine manufacturing operations, troubleshooting, requalification and continuous improvement initiatives with a focus on CIP, SIP and autoclave systems.

**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 ownerforCIP, SIP and AutoclaveDrug 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 degreeOR
- Mastersdegree and 2 years of Engineering experienceOR
- Bachelorsdegree and4years ofEngineeringexperienceOR
- Associatesdegree and8years ofEngineeringexperienceOR
- 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 limited domestic/international travel.

North Carolina

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. Amgen is advancing a broad and deep pipeline and portfolio of medicines to treat heart disease, obesity and obesity-related conditions, rare diseases, inflammatory conditions and cancer. 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 serve as part of the Drug Product Team (DPT) providing creative functional area strategies, crafting and executing DOEs during the development of pivotal and commercial ready programs.

This Amgen leader will apply deep expertise in organic molecules and their assemblies to develop innovative, accelerated approaches within cross-functional teams.

Collaborate across DPT and with partner functions, including Drug Substance Technologies, Attribute Sciences, Quality Assurance, Regulatory Affairs, Supply Chain, Contract Manufacturing, Pharmacokinetics and Drug Metabolism, Clinical Development, and Biostatistics.

Build effective working relationships within DPT and across Amgen functions, including Drug Substance Technologies, Attribute Sciences, Quality Assurance, Regulatory Affairs, Supply Chain, Contract Manufacturing, Pharmacokinetics and Drug Metabolism, Clinical Development, and Biostatistics.

Design and execute experiments.

Summarize results in technical documents, regulatory filings, and presentations.

Proactively engage with external industry groups, such as the IQ Consortium, and academic organizations, such as university consortia.

Provide technical expertise on the structure, reactivity, and physicochemical properties of materials, including drug substances and excipients.

**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 go getter with these qualifications.

**Basic Qualifications:**

Doctorate degree

OR

Masters degree and 2 years of **Scientific** experience

OR

Bachelors degree and 4 years of **Scientific** experience

**Preferred Qualifications:**

Ph.D. in a relevant scientific field such as Organic Chemistry, Physical Chemistry, Chemical Engineering, Materials Sciences, or Pharmaceutical Sciences

Strong scientific background for the deep understanding of the organic molecules and their assemblies.

Profound scientific acumen with a focus on organic chemistry, Physical Chemistry, solid-state chemistry, and the physicochemical properties of small molecules.

Industry experience: Prior work in the pharmaceutical sector, particularly with oral solid dosage forms.

Technical proficiency: Familiarity with a wide array of characterization techniques, including but not limited to XRPD, DSC, TGA, and SEM.

Patent process knowledge: Understanding of the patent application process and the legal framework governing patents is advantageous.

Manufacturing insights: Comprehensive knowledge of unit operations involved in producing oral solid dosage forms.

Research leadership: Ability to design, conduct, and complete independent formulation research.

Publication record: Demonstrated history of research dissemination through publications.

Team collaboration: Proven track record of effective cross-functional team engagement.

Writing excellence: Exceptional technical writing capabilities with meticulous attention to detail.

**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 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. We make all employment decisions without regard to race, color, religion, sex or any other characteristic protected by applicable law.

We provide reasonable accommodations to applicants and employees with disabilities, consistent with legal requirements. Please contact us to request accommodation.

Process Development Associate

**Join Amgens Mission of Serving Patients**

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

Since 1980, weve helped pioneer the world of biotech in our fight against the worlds toughest diseases. Amgen is advancing a broad and deep pipeline and portfolio of medicines to treat heart disease, obesity and obesity-related conditions, rare diseases, inflammatory conditions and cancer. 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 Associate**

**What you will do**

Lets do this. Lets change the world. Amgen is a leading biotechnology company with a mission to serve patients around the world. As a science-based, patient-focused organization, we discover and develop innovative therapies to treat serious illnesses.

Amgens Attribute Sciences (AS) department within the Process Development (PD) organization defines the favorable quality characteristics of the therapies it produces and optimizes innovative analytical tools to guide that development. The Pivotal PD organizations focus is developing and commercializing robust manufacturing processes across a wide range of therapeutic biologic modalities, including (but not limited to) monoclonal and bispecific antibodies, bispecific T-cell engagers (BiTEs), antibodydrug conjugates, live oncolytic viruses, and synthetic medicines.

As a PD Associate, the candidate will participate in protein characterization studies to support regulatory filings using Capillary Electrophoresis (CE), High Performance Liquid Chromatography (HPLC) / Ultra Performance Liquid Chromatography (UPLC) and mass spectrometry (MS). The candidate will also work to develop, qualify, and transfer analytical methods to Quality Control, and optimize and troubleshoot existing methods.

They will collaborate with other process development departments to support commercial process development and process characterization studies in support of marketing applications.

This position is located at our Thousand Oaks, CA site.

**Key responsibilities:**

Perform method development and qualification studies using HPLC, UPLC, and CE platforms

Perform chromatographic fractionation, peptide mapping, intact mass, and other LC-MS studies to support product characterization and comparability studies

Author results in laboratory notebooks and method development reports, interfacing closely with Attribute Sciences Team Leads and Quality Control to transfer and troubleshoot qualified methods

Participate in the maintenance of Attribute Sciences instruments and assist the Attribute Sciences department in maintaining a phase appropriate good manufacturing practices (GMP) environment

With a focus toward evaluation of critical quality attributes, coordinate and perform attribute identification and characterization studies, including isolation and analysis of chromatography fractions

Conduct and coordinate accelerated stability studies to define therapeutic degradative pathways

Perform evaluation of novel platform analytical technologies to help drive innovation

Perform experiments to help answer questions from health authorities

Collaborate with partner organizations during commercial process development, process characterization, and process validation studies to support marketing applications

**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:**

Bachelors degree

OR

Associates degree and 2 years of Scientific experience

OR

High school diploma / GED and 4 years of Scientific experience

**Preferred Qualifications:**

- Scientific background in method development and product characterization for therapeutic proteins
- Preferred Degree in Biochemistry, Analytical Chemistry, Protein Chemistry or related subject area
- Excellent written and verbal communication skills, ability to multitask, efficiently plan and follow through on complex projects
- A self-starter, and someone who values working in 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 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. We make all employment decisions without regard to race, color, religion, sex or any other characteristic protected by applicable law.

We provide reasonable accommodations to applicants and employees with disabilities, consistent with legal requirements. Please contact us to request accommodation.

Sr Associate IS Analyst - Process Development Labs

**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. Amgen is advancing a broad and deep pipeline and portfolio of medicines to treat heart disease, obesity and obesity-related conditions, rare diseases, inflammatory conditions and cancer. 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 Associate IS Analyst - Process Development Labs

**What you will do**

Lets do this. Lets change the world. In this vital role you will help create a reliable, secure technology environment for the scientists advancing our medicines. Based at Amgens Thousand Oaks, California facility, youll support the laboratory systems and instrument-connected computers scientists rely on every day. Youll partner with researchers and teams across IT to deploy and maintain lab technology, resolve user needs, keep systems current, and support data protection, backup, and archiving. Youll also help build and maintain tools and automation scripts that make the teams work more efficient. The role offers hands-on experience across lab technology, infrastructure, networking, and databasesand the opportunity to shape solutions that balance scientific needs, security, and enterprise priorities.

Youll join the Benchtop Product Team and support the full lifecycle of laboratory benchtop platforms across Operationsfrom software and hardware refreshes to ongoing system availability. Your work will help scientists stay focused on their research with dependable, up-to-date tools.

**Roles & Responsibilities**

- Partner with the Benchtop Product Team to manage the lifecycle of instrument controller software and laboratory computing platforms.
- Work with scientists and IS colleagues to resolve support requests involving laboratory computers, software and Windows upgrades, and system troubleshooting.
- Coordinate with vendors to obtain current controller software, drivers, patches, and other software packages.
- Collaborate with Amgen infrastructure teams to build and support DEV, TEST, and PROD environments in cloud and on-premises settings.
- Test software and hardware updates, develop migration strategies, and support the benchtop platforms in scope.
- Create and maintain documentation and standard operating procedures for lifecycle processes.
- Manage ServiceNow activities, including Service Access Reviews, application CI records, ISA/TPRA, end-of-life servers, and orphaned assets.
- Work with business partners to develop practical, innovative solutions to day-to-day challenges.

**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 Sr Associate IS Analyst with these qualifications.

**Basic Qualifications**

- Doctorate degree and 2 years of experience in Infrastructure, IT, or a related field; **or**
- Masters degree and 810 years of relevant experience; **or**
- Bachelors degree and 1014 years of relevant experience; **or**
- Diploma and 1418 years of relevant experience.

**Functional Skills**

**Required**

- 35 years of experience in systems administration and infrastructure.
- Strong customer focus and the ability to manage support requests in line with user expectations.
- Experience with networking, DNS, firewalls, security, patching, AWS, and VMware.
- A thorough understanding of Windows and Linux operating systems.
- Ability to define infrastructure requirements for different server types and assess vendor recommendations against business needs.
- Experience developing and maintaining scripts to automate server tasks.
- Proven leadership and organizational skills, including the ability to manage multiple software and hardware lifecycle projects.
- Ability to work with vendors and colleagues to troubleshoot issues, test software versions, and develop lasting solutions.

**Preferred Qualifications:**

- Ability to work independently, solve problems, and communicate professionally in writing.
- Experience with Smartsheet, Excel, or Tableau.
- Experience using generative AI tools such as ChatGPT or Copilot, and familiarity with large language models such as Llama.
- Experience working with business partners to shape and deliver solutions.

**Ways of Working**

- Experience leading technology transformation and managing change.
- Ability to collaborate effectively with global, distributed teams.
- Strong analytical, troubleshooting, and communication skills.
- Ability to manage competing priorities and take initiative.
- Confidence presenting information and speaking to groups.

**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 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. We make all employment decisions without regard to race, color, religion, sex or any other characteristic protected by applicable law.

We provide reasonable accommodations to applicants and employees with disabilities, consistent with legal requirements. Please contact us to request accommodation.

Manufacturing Process Technician -Material Management -Material Handler

**Join Amgen's Mission of Serving Patients**

Since 1980, we've helped pioneer the world of biotech in our fight against the world's 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, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller, happier lives.

Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lie within them, you'll 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 feature best-in-class drug substance manufacturing technologies with embedded Industry 4.0 capabilities and sustainability innovations designed to reduce carbon and waste.

**Manufacturing Process Technician -Material Management -Material Handler**

**Live**

**What you will do**

Lets do this! Lets change the world! In this dynamic role, you will be an Associate in the manufacturing organization at Amgen North Carolina (ANC). The essential position, which supports our critical 24/7 manufacturing operations, works a 12-hour 2-2-3 schedule from 5:45am to 6:15pm. In this role, you will support manufacturing operations by picking, delivering, and stocking cGMP materials and general consumables in accordance with standard operating procedures within a cGMP environment.

With specific instruction and under supervision, the Material Handler performs hands-on material movement and inventory activities while maintaining strict safety, compliance, documentation, and customer-service standards. The Material Handler will support all floor operations in accordance with cGMP practices. As Amgen relies upon the regular attendance of staff members to meet legitimate business needs, staff must be able to work assigned 12-hour shifts, including during inclement weather, some holidays and requested overtime in support of our 24/7 operations.

**Responsibilities will include...**

**Safety / Compliance**

- Pick, deliver, and stock cGMP floor-stock materials and general consumables.

- Perform work in accordance with established standard operating procedures (SOPs), cGMP requirements, applicable Code of Federal Regulations (CFR), Amgen policies, and OSHA regulations.

- Maintain compliant training records and follow proper gowning requirements.

- Maintain a clean and safe work area.

- Report safety hazards immediately to leadership.

**Systems**

- Use inventory systems to complete routine transactions and resolve basic system issues within Amgen enterprise resource planning systems, including SAP and MES.

- Use quality, operations, and logistics software applications with appropriate read and write access.

- Review and verify cGMP transactions.

- Manage inventory by removing expired materials from cGMP areas and completing the appropriate MES and SAP transactions.

**Equipment**

- Use powered industrial vehicles (PIVs) to move warehouse materials.

- Conduct pre-operational safety inspections of PIVs.

- May operate trucks to move warehouse materials, hazardous materials, or general consumables.

- Operate warehouse equipment as assigned, including forklifts, pallet jacks, special-purpose cryogenic equipment, and potent-compound equipment.

**Collaboration and Work Practices**

- Interact constructively with peers and internal clients.

- Provide basic customer service and prioritize work to meet deadlines.

- Work effectively in a fast-paced team environment, both independently and as part of a team.

- Perform other functions as assigned.

**Win**

**What we expect of you**

We are all different, yet we all use our unique contributions to serve patients. The dependable professionals we seek are team players with these qualifications.

**Basic Qualifications:**

- High school diploma / GED + 1 year of manufacturing and/or other regulated experience

- Or

- Associates degree

**Preferred Qualifications**

- Experience working in a cGMP environment.

- Experience with SAP, MES, inventory systems, or related quality, operations, and logistics software.

- Experience safely operating trucks, vans, powered industrial vehicles, forklifts, pallet jacks, or other warehouse equipment.

- Experience safely handling, transporting, and managing hazardous materials.

- Keen attention to detail and the ability to accurately follow complex written procedures.

- Ability to assemble, disassemble, operate, and understand complex equipment or processes in accordance with procedures.

- Strong computer skills and the ability to work efficiently across multiple software applications.

- Intermediate mathematical skills.

- Good written and verbal communication skills.

- Good problem-solving skills and the ability to prioritize work to meet deadlines.

- Ability to understand and adhere to cGMP requirements.

- Demonstrated alignment with Amgen values.

**Physical Requirements**

- Stand, walk, or move throughout offices, work sites, and Amgen buildings.

- Climb, crawl, crouch, or work in other non-seated positions.

- Lift, carry, push, or pull heavy objects using appropriate industrial equipment.

- Maintain the visual and mental concentration needed to work with specialized equipment and instruments.

**Thrive**

**What you can expect of us**

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

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors, including relevant skills, experience, and qualifications.

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

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

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

- Stock-based long-term incentives.

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

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

**Apply now**

**for a career that defies imagination**

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

Manufacturing Process Tech - Solution Prep (Nights)

**Join Amgens Mission of Serving Patients**

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

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

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

**Manufacturing Process Technician - Solution Prep (Nights)**

**What you will do**

Lets do this! Lets change the world! In this vital role you will routinely perform simple to moderately complex processes according to Standard Operating Procedure and Batch Records. Generally, this will include all aspects associated with bulk manufacturing in aseptic and non-aseptic environments.

Responsibilities:

- Equipment and parts cleaning using manual and automated methods and equipment
- Set up and breakdown of single use materials
- Weigh and dispense of raw materials
- Operation and process monitoring of clean systems, autoclaves, and processing equipment
- Sample collection, processing, storage and delivery
- Product and component reconciliation
- Solution preparation and transfer
- Materials handling, weighing and dispensing, power industrial vehicle operation
- Strict adherence to current Good Manufacturing Practices (cGMP's), responsible to accurately complete process-associated documentation, make calculations and perform the physical tasks associated with bulk manufacturing and other duties as assigned.

You will be expected to join a shift team working a 12-hour shift. The shift pattern will be 7am-7pm with a two-week rotation covering 7 days per week. The rotating shift offers several benefits, with an average of 14 days on shift per month with every other weekend off as well as **receiving an added 15% shift differential.** The schedule during the initial on-boarding phase for this role (2-6 weeks) will be administrative (Monday through Friday, approximately 8am to 5pm).

**What we expect of you**

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

**Basic Qualifications:**

- High school/GED + 1 year of Manufacturing or Operations work or military experience OR
- Associate's degree

**Preferred Qualifications:**

- Experience in a GMP/ other regulated environment.
- Demonstrated knowledge of GMP principles.
- Drug substance manufacturing experience.
- Ability to stand or sit for extended periods of time.
- Ability to maintain focus during repetitious tasks over the course of a shift.
- Ability to assemble, disassemble, operate and understand simple to moderately complex equipment per procedures.
- Basic understanding of measurements, calculations and the metric system.
- Ability to work effectively in an individual and team setting.
- Ability to document process tasks in electronic batch records.
- Coachable, ability to take coaching/critique and show learned/measurable improvement.
- Capacity to follow written procedures, recognize and report malfunctions.
- Strong communication skills.
- Ability to perform assignments with a high degree of focus/attention to detail.

**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 Associate 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 Associate Scientist**

**What you will do**

Lets do this. Lets change the world. As a Process Development Associate Scientist, you will play an integral part in Amgens Late-Stage Synthetics and Commercial Drug Product team within the Drug Product Technologies department. Your responsibilities will center around gaining practical experience and offering hands-on expertise in formulation and process development for Amgens synthetics pipeline. The core activities of this group involve developing clinical, robust commercial formulations and life cycle management initiatives for a wide array of Amgens synthetic assets.

This position provides the unique opportunity to collaborate with skilled scientists and contribute to the advancement and launch of innovative synthetic drug products across a variety of oral or parenteral dosage forms. Through your work, you will support both the development and commercialization phases, ensuring that Amgen continues to deliver cutting-edge solutions for patients worldwide.

- Hands-on experience in spray-drying formulation and process development, including experimental design, process optimization, data analysis, and characterization of spray-dried materials.

- Understanding of spray-drying process scale-up from laboratory to manufacturing scale, including equipment considerations, technology transfer, process troubleshooting, and identification of critical process parameters and quality attributes.

- Interface within the Drug Product Technologies Department as a team member to support programs and initiatives.

- Contribute to the completion of experimental design and execution and assist in the analysis and interpretation of data.

- Utilize digital tools and emerging AI-enabled solutions to improve experimental efficiency, data analysis, and scientific insight generation.

- Contribute to technical problem-solving efforts and identify opportunities for automation and digital solutions to improve efficiency and reduce repetitive manual tasks.

- Actively contribute to process improvements, strategy development, and cross-functional partnerships that promote consistent and efficient practices across late-stage clinical and commercial synthetic programs.

- Organize and communicate information within the team to help lead to the best possible formulation and processes.

**What we expect of you**

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

**Basic Qualifications:**

- Masters degree and 1 years of scientific experience

- OR

- Bachelors degree and 3 years of scientific experience

**Preferred Qualifications:**

- Masters degree in Pharmaceutical Sciences, Chemical or Pharmaceutical Engineering, Chemistry, or a life sciences-related field, with relevant industry experience.

- Understanding of the typical unit operations for the manufacture of oral solid dosage forms (i.e., granulation, roller compaction, drying, milling, blending, compression, film coating, etc.).

- Basic understanding of the physical and chemical stability of synthetic molecules, enabling formulations, amorphous solid dispersions, and how manufacturing processes, including spray drying, HME, roller compaction, and compression, impact product quality.

- Ability to design, execute, and interpret experimental results.

- Strong problem-solving skills applied to the formulation and characterization of parenteral and oral synthetic molecules.

- Excellent written and verbal communication skills for presenting scientific results in a fast-paced, multi-disciplinary environment.

- Proven ability to work effectively in collaborative, team-based settings.

- A proactive, curious, and innovative mindset, with enthusiasm for applying digital solutions to scientific challenges

**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 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 Scientist**

**What you will do**

Lets do this. Lets change the world. In this vital role you will join the Drug Product Technologies (DPT) in Thousand Oaks, California, is seeking a Process Development Scientist to support early clinical development of oral drug products for synthetic molecules. This hands-on laboratory position will focus on formulation and process development for platform immediate-release (IR) tablets and enabling formulations, including amorphous solid dispersions (ASDs). Process characterization will support early clinical supply across these formulations. GMP manufacturing will focus primarily on enabling formulations, particularly ASDs, while also supporting platform IR tablets as needed.

**Key Responsibilities**

Develop and optimize oral drug product formulations and processes for early clinical studies, including platform IR tablets and enabling formulations.

Conduct laboratory studies to characterize materials and formulations, assess process performance, and establish manufacturable approaches.

Collaborate with colleagues across DPT and partner functions, including Drug Substance Technologies, Attribute Sciences, Regulatory Affairs, Supply Chain, Pharmacokinetics and Drug Metabolism, Clinical Pharmacology, and Biostatistics, as well as external manufacturing partners and academic groups.

**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
- OR
- Masters degree and 2 years of Scientific experience
- OR
- Bachelors degree and 4 years of Scientific experience

**Preferred Qualifications:**

Hands-on GMP manufacturing experience with amorphous solid dispersions (ASDs) produced by hot-melt extrusion (HME) and/or spray-dried dispersion (SDD), including development of manufacturing procedures.

Hands-on GMP experience with roller compaction and tablet compression for immediate-release (IR) tablets.

Experience identifying and troubleshooting issues during GMP processing.

Academic or professional background in pharmaceutical sciences, materials science, bioengineering, or an engineering discipline.

In-depth understanding of pharmaceutical material science and how material properties affect formulation development, process performance, and manufacturability for early clinical programs.

Experience supporting FIH drug product development, including formulation and process development for immediate-release (IR) tablets.

Experience working with contract research or manufacturing organizations.

Experience preparing or contributing to regulatory documentation, such as IND CMC sections, and interacting with regulatory authorities.

Strong communication and collaboration skills, including the ability to work across functions and resolve project-related issues.

Experience with physiologically based biopharmaceutics modeling tools such as GastroPlus or Simcyp.

**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.