Scientist, Pharmaceutical Science/ Research, Research Scientist
Job in
Thousand Oaks, Ventura County, California, 91362, USA
Listed on 2026-10-05
Listing for:
JobDiva, Inc.
Full Time
position Listed on 2026-10-05
Job specializations:
-
Research/Development
Pharmaceutical Science/ Research, Research Scientist -
Pharmaceutical
Pharmaceutical Science/ Research
Job Description & How to Apply Below
100% Onsite - HQ-Thousand Oaks (USTO)
The Scientist, Attribute Sciences, Process Development develops, qualifies, and transfers phase-appropriate analytical methods supporting small molecule drug substance and drug product development from early clinical through commercial stages. The role collaborates closely with Process Development DS/DP teams to ensure methods are scientifically sound and compliant with regulatory requirements.
Education- Ph.D. in Analytical Chemistry, Pharmaceutical Sciences, Chemistry, or related scientific discipline with 1–3 years of industry experience;
- M.S. with 4–6 years of relevant pharmaceutical industry experience;
- B.S. with 6–8 years of relevant pharmaceutical industry experience.
- Hands‑on experience with HPLC/UHPLC, GC, LC‑MS, dissolution, KF, UV‑Vis, FTIR, particle size, ICP‑MS, and related analytical techniques.
- Strong knowledge of method development, qualification, validation, and transfer.
- Experience with impurity characterization, stability studies, and DS/DP development support.
- Develop, optimize, troubleshoot, and qualify analytical methods for characterization, release, stability, and process support.
- Develop stability‑indicating methods for critical quality attributes, including assay, impurities, dissolution, water content.
- Support process development, optimization, technology transfer, and control strategy development.
- Characterize intermediates, starting materials, drug substances, and drug products.
- Build process understanding through impurity profiling and material characterization.
- Plan and execute method qualification and validation in accordance with ICH guidelines.
- Ensure methods are robust, reproducible, and fit for purpose across the product lifecycle.
- Analyze experimental data using sound scientific and statistical approaches.
- Maintain accurate documentation in ELNs and laboratory information systems.
- Author technical reports, development summaries, protocols, and presentations.
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