Associate Scientist, Small Molecule Formulation & Process Development

Biopharma Careers

Foster City (CA)

On-site

USD 110,000 - 142,000

Full time

6 days ago
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Job summary

Gilead Sciences Inc. is seeking an Associate Scientist within the FPD group in Foster City, CA. The role supports formulation development, manufacturing process development, and tech transfer from development through scale-up at internal and external sites.

The candidate will help establish robust DP formulation strategies and contribute to regulatory filings from IND to NDA. The position involves performing and overseeing GMP clinical manufacturing and cross-functional collaboration, with

Qualifications

  • BS degree in related scientific discipline with 5+ years of experience or MS degree with 3+ years of experience.
  • Experience must be in related scientific discipline.

Responsibilities

  • Organizes, files and retrieves project-related records.
  • Maintains the proper functions of laboratories.
  • Operates laboratory instrumentation and/or processing equipment and can train others to conduct low to moderate complexity experiments.
  • Designs and executes low to moderate complexity experiments in support of cross-functional projects.
  • Troubleshoots analytical methods, instrument operation, manufacturing and experimental design.
  • Performs drug substance, drug product intermediate and drug product characterization.
  • Oversees routine GMP clinical manufacture of drug products and/or development batches.
  • Works collaboratively with peers from other departments and external partners.
  • Summarizes experimental results and presents conclusions in team meetings and department presentations.
  • Authors templated memos and reports. Authors medium complexity.

Education

BS degree in related scientific discipline
MS degree in related scientific discipline

Job description

Gilead Sciences Inc. is seeking an Associate Scientist within the FPD group in Foster City, CA. The role supports formulation development, manufacturing process development, and tech transfer from development through scale-up at internal and external sites.

The candidate will help establish robust DP formulation strategies and contribute to regulatory filings from IND to NDA. The position involves performing and overseeing GMP clinical manufacturing and cross-functional collaboration, with

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