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Amgen

Makes biotech medicines for serious illnesses

Process Development Senior Scientist

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeThousand Oaks, CA, USA

About the Job

Requirements

  • A doctorate degree (PhD, PharmD, or MD), with relevant postdoctoral experience where applicable; or a master's degree and 3 years of scientific experience; or a bachelor's degree and 5 years of scientific experience.
  • Preferred: PhD in Pharmaceutics, Biotechnology, Chemical Engineering, Bioengineering, Biochemistry, or a related field, with 2–4 years of postdoctoral or industry experience.
  • Experience integrating formulation, stability, and analytical data to advance biologics, including enzyme, monoclonal antibody, and peptide candidates, is highly desirable.
  • Demonstrated understanding of biologics drug product development considerations, including protein stability, degradation pathways, quality attributes, and product/process comparability.
  • Experience developing or characterizing enzymes, including assessment of activity, stability, and performance under relevant formulation or process conditions.
  • Experience in formulation and co-formulation development, fill-finish process engineering, technical transfers to global manufacturing sites, statistical process control, and statistical design and analysis of experiments.
  • A strong foundation in analytical and biophysical techniques relevant to biologics, such as ultra-performance liquid chromatography, high-performance liquid chromatography, size-exclusion chromatography, ion-exchange chromatography, reverse-phase high-performance liquid chromatography, hydrophobic interaction chromatography, capillary electrophoresis sodium dodecyl sulfate, and subvisible particle analysis.
  • Experience with programming, artificial intelligence-enabled tools, and data visualization tools such as Tableau and Spotfire.
  • Experience contributing to regulatory submissions, including clinical trial applications and biologics license applications.
  • Strong project management skills, including the ability to manage project resources such as materials, workforce, and time.
  • Critical thinking, problem-solving, and independent research skills.
  • Ability to work effectively in a fast-paced, matrixed environment and collaborate cross-functionally.

Responsibilities

  • Participate in drug product commercialization teams conducting process development for pipeline products and supporting commercial products through lifecycle management.
  • Design, plan, complete, and document formulation and process development studies.
  • Apply scientific and engineering principles and techniques to develop, characterize, and implement processes and next-generation technologies, and to solve technical challenges.
  • Apply advanced statistical and data analytics techniques to draw conclusions and inform decisions.
  • Develop and characterize liquid formulations for biologics, with particular emphasis on enzyme drug product formulation or co-formulations.
  • Build process understanding across unit operations to support scalable drug product development.
  • Apply machine learning, artificial intelligence, and data science to predictive modeling, workflow acceleration, and decision-making.
  • Author and review guideline documents, technical protocols and reports, risk assessments, and regulatory sections supporting investigational new drug and marketing application submissions.
  • Support clinical and commercial technology transfer activities and manufacturing operations through process fit assessments, process capability analysis, troubleshooting, root cause analysis, and product impact assessments for process changes, improvements, and non-conformance investigations.
  • Stay current on industry and scientific developments to support ongoing innovation and future business needs.
  • Communicate with management, cross-functional partners, and relevant team members about progress and forthcoming program needs.
  • Lead cross-functional initiatives that enhance drug product platforms and contribute to process design improvement projects.

About the Company

Amgen

Makes biotech medicines for serious illnesses

Amgen develops and makes biologic medicines, which are drugs built from proteins and antibodies grown in living cells, for serious conditions such as heart disease, cancer, and bone loss. Its anemia drug Epogen, approved in 1989, became one of the biotechnology industry's first blockbuster medicines. Amgen grows these drugs in large tanks called bioreactors, and its products include the cholesterol drug Repatha, the bone-building drug Evenity, and the severe asthma drug Tezspire. It earns money by selling these medicines, mostly through large drug wholesalers that supply hospitals and pharmacies. Amgen was founded in 1980 and is based in Thousand Oaks, California.

Company size
10,001+
Company stage
IPO
Headquarters
Thousand Oaks, CA
Founded
1980

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