Process Development Associate Scientist – Commercial Support Full-time NEW

Join Amgen's Mission of Serving Patients

At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.

Since 1980, we've helped pioneer the world of biotech in our fight against the world's 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, 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 lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

Process Development Associate Scientist – Commercial Support

What you will do

Let's do this. Let's change the world! In this vital role, you will join the Drug Substance Cell Sciences and Engineering team to provide support to Amgen's manufacturing plants. You will contribute to process development, process improvement, investigations, technology transfers, and other projects that support reliable manufacturing and delivery of life-changing therapies to patients.

Specific responsibilities include but are not limited to:

• Support process improvement initiatives, technology transfers, and implementation of data-driven solutions to enhance Drug Substance manufacturing processes.
• Investigate deviations, perform root cause analysis, and support the implementation of corrective and preventive actions (CAPAs).
• Develop, optimize, and troubleshoot scientific methods, processes, and protocols to meet project and business objectives.
• Author and review technical documents, protocols, reports, presentations, and regulatory support documentation.
• Stay current on scientific literature, emerging technologies, and industry best practices, and apply relevant insights to projects and operations.
• Partner with Manufacturing, Quality, Engineering, Process Development, and other cross-functional teams to drive project execution and operational excellence.
• Analyze, interpret, and present data-driven findings, technical conclusions, and recommendations to stakeholders.
• Ensure compliance with safety, quality, regulatory, and cGMP requirements in all activities and deliverables.
• Contribute to departmental initiatives, including safety, continuous improvement, training, recruiting, and knowledge-sharing activities.

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The Process Development Scientist professional we seek is a collaborative and technically strong individual contributor with these qualifications.

Basic Qualifications:

Master's degree and 1 year of scientific, process development, laboratory, or manufacturing support experience

OR

Bachelor's degree and 3 years of scientific, process development, laboratory, or manufacturing support experience

Preferred Qualifications:

• Bachelor's degree in Life Sciences, Biotechnology, Chemical Engineering, Biochemical Engineering, Biology, Chemistry, or a related scientific or engineering discipline.
• Experience in biopharmaceutical process development, Drug Substance manufacturing support, cell culture, process characterization, technology transfer, and/or process improvement.
• Working knowledge of mammalian cell culture and/or bacterial fermentation processes, including bioreactor operations, harvest processes, and associated process controls.
• Understanding of cGMP-regulated manufacturing environments, quality systems, and regulatory requirements.
• Experience supporting deviation investigations, troubleshooting, root cause analysis, product impact assessments, contamination assessments, and CAPA implementation.
• Strong technical and analytical skills, including scientific data interpretation, statistical analysis (e.g., JMP), process monitoring, and data-driven decision-making.
• Ability to evaluate process performance, identify improvement opportunities, and implement effective solutions.
• Strong organizational, project management, and documentation skills, with the ability to manage multiple priorities and meet timelines.
• Effective written and verbal communication skills, including technical writing and presentation of scientific data to cross-functional teams.
• Bilingual proficiency in English and Spanish, both written and verbal.
• Demonstrated ability to collaborate across functions, adapt to evolving business needs, and thrive in a fast-paced environment.
• Flexibility to support non-standard schedules, on-call responsibilities, and manufacturing operations, as required.

What you can expect of us

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

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

• A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental & vision coverage, and life & disability insurance
• 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 an annual site shutdown
• 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.