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Senior Scientist, Analytical Chemistry
Job in
Edison, Middlesex County, New Jersey, 08818, USA
Listed on 2026-09-12
Listing for:
Scorpion Therapeutics
Full Time
position Listed on 2026-09-12
Job specializations:
-
Healthcare
-
Science
Research Scientist
Job Description & How to Apply Below
The Senior Scientist, Analytical Chemistry supports analytical development, validation/verification, and method transfer for the Quality Control laboratory to characterize drug substance, raw materials, and drug products.
Essential Functions:- Develop and validate analytical methods (mostly LC and GC) for APIs, excipients, and dosage forms for routine analysis; optimize and qualify new/existing methods.
- Perform physical and chemical analysis of raw materials, in-process, finished products, and stability samples per written methods, specifications, and SOPs; comply with cGMP and state/federal regulations.
- Use and calibrate analytical instruments (e.g., sonic sifter, laser diffraction, Karl Fischer, UV-Vis, FTIR, HPLC with UV/conductivity, TLC, pH meter, dissolution apparatus) and related equipment.
- Provide timely responses to internal/external inquiries.
- Train and guide analysts; expand analytical capabilities.
- Execute and document analyses; calculate/report results; investigate and review data for completeness and specification compliance.
- Evaluate, recommend, and implement new analytical technologies and instrumentation.
- Stay current on analytical technology developments; improve lab efficiency and GMP compliance.
- Lead team members on assigned projects.
- Participate/lead scientific discussions with cross-functional teams.
- Education:
BS/BA in chemistry or relevant pharmaceutical sciences (Required); MS/MA (Preferred). - Experience:
5+ years pharmaceutical experience with BS/BA; 4+ years with MS/MA. - Specialized Knowledge/
Skills:
In-depth analytical chemistry (spectrophotometric, dissolution/drug release, chromatographic, physical parameter measurements), ability to follow USP/EP/BP/JP procedures and apply cGMP; advanced troubleshooting; trend identification in analytical data; hands‑on HPLC, GC, dissolution, UV, FTIR, TLC, MS; method development/validation; experience writing SOPs and test methods; regulatory document compilation experience.
- Base salary range: $90,000–$123,000/year; short-term incentive/bonus opportunity within first 12 months. Benefits include health/insurance and 401(k) match (for eligible positions).
Position Requirements
10+ Years
work experience
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