Review third-party certificates of analysis (RP-HPLC with UV detection) and check each lot's reported results against its specification. Coordinate lot testing with independent laboratories and keep lot documentation current, so every product page links the COA on file or shows COA pending.
Requirements
- B.S. or M.S. in Chemistry, Biochemistry, or related field
- Experience interpreting HPLC and LC-MS data
- Familiarity with GMP or cGMP environments preferred
- Detail-oriented with strong documentation skills