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Senior Scientist – Drug Product Development

Job in Novato, Marin County, California, 94949, USA
Listing for: Tucker Parker Smith Group (TPS Group)
Full Time position
Listed on 2026-07-15
Job specializations:
  • Pharmaceutical
    Pharmaceutical Science/ Research, Pharmaceutical Manufacturing
Salary/Wage Range or Industry Benchmark: 150000 - 175000 USD Yearly USD 150000.00 175000.00 YEAR
Job Description & How to Apply Below

Overview

Senior Scientist – Drug Product Development.

Location:

Novato, CA (Hybrid – 2–3 days onsite). Salary: $150,000–$175,000 annually + Comprehensive Benefits.

Employment Type:

Full-Time.

Responsibilities
  • Lead drug product development for small molecules, peptides, and oligonucleotides.
  • Develop formulation strategies, optimize drug products, and support technology transfer and manufacturing.
  • Lead cross-functional CMC teams, collaborating with Analytical Development, Manufacturing, Quality, Regulatory, Packaging, Engineering, and external CDMOs.
  • Drive project timelines, manage technical risks, and ensure successful program execution.
  • Provide scientific oversight for formulation development, manufacturing support, process optimization, and technology transfer activities.
  • Support regulatory submissions by contributing to CMC documentation and technical reports.
  • Mentor junior scientists and provide technical leadership across multidisciplinary teams.
Qualifications
  • Master's or Ph.D. in Pharmaceutics, Pharmaceutical Sciences, Biochemistry, Chemical Engineering, or a related scientific discipline.
  • 7–10+ years of pharmaceutical or biotechnology industry experience in drug product development.
  • Strong expertise in formulation development and CMC activities.
  • Hands-on experience with solid oral dosage forms
    , including tablets, capsules, and oral solutions.
  • Experience leading cross-functional teams and collaborating with CDMOs/CMOs.
  • Experience supporting technology transfer, manufacturing, and regulatory submissions.
  • Working knowledge of GMP regulations and pharmaceutical development.
Preferred Qualifications
  • Experience with parenteral formulations and fill/finish operations.
  • Experience with small molecules, peptides, oligonucleotides, or biologics.
  • Familiarity with analytical techniques including HPLC, DSC, UV spectroscopy, DLS, particle size analysis, and stability testing.
Benefits

This is an outstanding opportunity to lead innovative drug product development programs from concept through commercialization while working alongside highly collaborative scientific teams. You'll have the opportunity to influence technical strategy, solve complex development challenges, and contribute to therapies that have the potential to improve patients' lives.

If you're passionate about drug product development and are looking for your next leadership opportunity, we'd love to hear from you!

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Position Requirements
10+ Years work experience
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