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Associate Director​/Principal Scientist

Job in Foster City, San Mateo County, California, 94420, USA
Listing for: Gilead Sciences, Inc.
Full Time position
Listed on 2026-01-12
Job specializations:
  • Engineering
    Research Scientist, Process Engineer, Biotechnology
Salary/Wage Range or Industry Benchmark: 200000 - 250000 USD Yearly USD 200000.00 250000.00 YEAR
Job Description & How to Apply Below

Associate Director/Principal Scientist

United States - California - Foster City Process/Product Development & Operations Regular

The Associate Director/ Principal Scientist , Cell Culture Process Development (Pivotal & Commercial), will be responsible for leading aspects of cell culture development including commercial process development and process characterization for multiple biologics programs during pivotal phases (phases II/III and post-launch). In addition, this role is also expected to lead projects for cell culture process technology development, platform process evolution, and to support cell culture-related regulatory documentation.

Key Responsibilities
  • Optimize and characterize cell culture processes to supply pivotal trials and enable commercialization for monoclonal antibodies, multi‑specifics, and novel modalities.
  • Lead and/or support entire lifecycle of pivotal activities including process risk assessment, process characterization, preparation of all supporting documentation/reports toward BLA submission, provide support to ensure successful process performance qualifications (PPQ), and author relevant sections of BLA.
  • Lead and/or support technology transfer and investigation activities in partnership with the global manufacturing sciences and technologies (MSAT) group.
  • Design experiments and perform hands‑on cell culture operations in shake flasks, ambr
    15, ambr
    250, bench‑scale bioreactors, and novel cell culture platforms.
  • May provide support to pilot plant operation for up to 500 L single‑use bioreactor.
  • Perform statistical analyses and appropriate modeling to assess process parameter criticality, identify acceptable ranges, and contribute to integrated control strategy.
  • Author and review GMP and non‑GMP technical documents (reports, regulatory submissions/responses, batch records, SOPs etc.), present in group/cross‑functional meetings.
  • Participate and work cross‑functionally within and outside of biologics technical development to achieve common goals.
  • Explore, develop, and implement novel cell culture technologies to meet business needs.
  • Manage direct and indirect reports and mentor junior group members while working in a flexible and agile environment.
  • Some travel may be required to support technology transfers and provide oversight at external manufacturing facilities.
  • Adhere to department budget and all training, compliance and safety requirements.
  • Remain current on trends and new technology advancements across the Biopharmaceutical industry.
  • Hire, mentor and develop team members within the organization to help build and grow a world‑class biologics cell‑culture process development organization.
Qualifications
  • Ph.D. with 5+ years OR M.S. with 8+ years OR B.S. with 10+ in a relevant scientific discipline (biology, bioengineering, chemical engineering, biochemical engineering).
  • Experience leading pivotal stage cell culture process development/characterization and implementation in GMP facilities.
  • Experience in building high‑performing teams through strategic coaching and feedback.
  • Hands‑on laboratory operations experience including shake flask, high‑throughput bioreactor, bench scale bioreactor, and pilot scale cultures.
  • Excellent communication, technical writing, and presentation skills and aptitude for creative problem solving.
  • Demonstrated ability to collaborate and influence cross‑functionally.
  • Experience in cell culture media development, and/or employing modeling techniques for upstream process development and optimization is preferred.
  • Experience in statistics, design‑of‑experiments, and data analysis (e.g. JMP, Spotfire).
  • Working knowledge of lab automation, data management, data science, knowledge management and data protection.
  • Experience with viral vaccines is a plus.
  • Passion for inclusion: knowing the business value of diverse teams, modeling inclusion, and embedding the value of diversity in the way he/she/they work.
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Position Requirements
10+ Years work experience
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