Overview In this role you apply Intermediate-level expertise in analytical chemistry and chromatography to execute tests and support senior staff. You will troubleshoot instrumentation and document findings while contributing to method validation and transfers. You guide Associate Scientists and help ensure GMP-compliant laboratory practices. This position offers exposure to a range of instruments and data systems in a regulated pharma environment.
Responsibilities- Perform routine analytical testing using instrumental methods (HPLC, GC, FTIR, UV, ICP-MS) with emphasis on chromatography
- Update and route SOPs, MOAs, and specifications for USP compliance
- Support method validation, verification, transfers, and evaluations
- Troubleshoot instrumentation and research literature or vendors when needed
- Provide guidance to Associate Scientists
- Assist in training laboratory personnel on GMP, safety, and new employee onboarding
- Maintain accurate project records and document testing per Good Documentation Practices
- Peer-review data to ensure accuracy and compliance
- Manage work/time according to departmental priorities
Key requirements- Bachelor in Chemistry or Biology or equivalent physical science
- 1-4 years of related pharmaceutical industry experience
- Familiarity with cGMP and FDA regulations
- Hands-on experience with chromatographic methods and chromatography data systems (e.g., Empower)
- Proficient in Microsoft Office (Word, Excel)
- Some method development experience and strong troubleshooting knowledge is desirable
- Flexibility with changing projects and priorities
- Clear communication with management and peers
- Problem-solving and analytical mindset
- Team guidance and training ability
- Chromatographic methods: HPLC, GC, FTIR, UV, ICP-MS
- Chromatography data systems (Empower)
- Method validation and verification
