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Scientist​/Senior Engineer – Drug Product Process Engineering

Job in Thousand Oaks, Ventura County, California, 91362, USA
Listing for: Amgen
Full Time position
Listed on 2026-07-09
Job specializations:
  • Engineering
    Process Engineer, Validation Engineer, Quality Engineering, Chemical Engineering
Salary/Wage Range or Industry Benchmark: 90000 - 130000 USD Yearly USD 90000.00 130000.00 YEAR
Job Description & How to Apply Below
Position: Scientist/ Senior Engineer – Drug Product Process Engineering

Scientist/ Senior Engineer – Drug Product Process Engineering

In this role you will serve as Process Engineering Lead providing technical and project leadership for drug product formulation, fill/finish, inspection, and presentation‑specific activities. The position supports clinical and commercial manufacturing operations, technology transfers, new product introductions, process characterization, optimization, and product impact assessments. It requires close collaboration with cross‑functional partners across Process Development, Manufacturing, Quality, Regulatory, Attribute Sciences, Engineering, Supply Chain, and Commercial Operations.

Responsibilities
  • Serve as the Drug Product SKU Lead for assigned commercial or late‑stage pipeline products, providing end‑to‑end technical ownership for formulation, fill/finish, presentation, and lifecycle management activities.
  • Lead or support commercial technology transfers, including facility‑fit assessments, make‑a‑batch assessments, process gap analyses, risk assessments, process characterization studies, technical documentation, and on‑site manufacturing support.
  • Act as a Process Engineering Lead for parenteral drug product unit operations, including formulation, mixing, sterile filtration, filling, capping, lyophilization, visual inspection, and related equipment/process interfaces.
  • Plan, design, execute, and document laboratory, offline, and on‑site studies related to drug product process development, process characterization, scale‑up, process robustness, and lifecycle management.
  • Provide technical leadership for assigned SKUs by integrating process understanding, product quality attributes, manufacturing performance, analytical data, regulatory commitments, and site capabilities.
  • Support clinical and commercial manufacturing operations through process capability analysis, troubleshooting, root cause analysis, non‑conformance investigations, corrective and preventive actions, and product impact assessments.
  • Author and review technical protocols, study reports, process transfer documents, product impact assessments, regulatory submission sections, responses to regulatory questions, and lifecycle management documentation.
  • Partner with manufacturing sites and cross‑functional teams to assess and implement process changes, equipment changes, raw material changes, scale changes, site transfers, and process improvements while ensuring product quality and supply continuity.
  • Apply scientific and engineering principles, including biochemistry, biophysics, statistics, chemical engineering, mechanical engineering, automation, and equipment design, to solve complex technical challenges.
  • Use data‑driven approaches, statistical analysis, process monitoring, modeling, and advanced digital or AI‑enabled tools to improve process understanding, manufacturing robustness, and technology transfer efficiency.
  • Lead or participate in global cross‑functional teams in a highly matrixed environment, influencing decision‑making, communicating risks, and driving alignment across stakeholders.
  • Deliver clear technical updates, progress reports, risk assessments, and recommendations to management, program teams, governance forums, and manufacturing partners.
  • Build and sustain strong partnerships with Drug Product Technologies, Attribute Sciences, Manufacturing, Quality, Regulatory, Engineering, Supply Chain, and site teams to ensure alignment between product needs, process requirements, and site capabilities.
Basic Qualifications
  • Doctorate degree
  • Or Master’s degree and 2 years of Operations, Process Development, Scientific, or Engineering experience
  • Or Bachelor’s degree and 4 years of Operations, Process Development, Scientific, or Engineering experience
Preferred Qualifications
  • M.S. or Ph.D. in Chemical Engineering, Biomedical Engineering, Pharmaceutical Sciences, Pharmaceutics, Chemistry, Biochemistry, Biotechnology, Material Science, or a related technical discipline.
  • 3+ years of experience in drug product process development, process engineering, commercialization, manufacturing sciences, or lifecycle management within the pharmaceutical or biotechnology industry.
  • Experience supporting…
Position Requirements
10+ Years work experience
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