Scientist, Pharmaceutical Science/ Research, Drug Discovery
Listed on 2026-08-15
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Pharmaceutical
Pharmaceutical Science/ Research, Drug Discovery, Analytical Chemist -
Research/Development
Pharmaceutical Science/ Research, Drug Discovery, Research Scientist
Scientist, Attribute Sciences, Process Development
The Scientist, Attribute Sciences, Process Development develops, qualifies, and transfers phase-appropriate analytical methods supporting small molecule and antibody-drug conjugate (Client) 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; or M.S. with 4–6 years of relevant pharmaceutical industry experience; or B.S. with 6–8 years of relevant pharmaceutical industry experience.
Required Technical
Experience:
Hands-on experience with HPLC/UHPLC, LC-MS/MS, GC, KF, UV-Vis, FTIR, and related analytical techniques. Strong knowledge of method development, qualification, validation, and transfer. Experience supporting small molecule and antibody-drug conjugate (Client) development including impurity characterization, stability studies, and DS/DP analytical activities.
Key Responsibilities:
- 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 small molecule and Client process development, optimization, technology transfer, and control strategy development.
- Characterize intermediates, starting materials, drug substances, and drug products for small molecules and Client programs.
- 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, p
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