QC Analytical Chemist
About The Position
Eurofins Professional Scientific Services (PSS) is hiring a QC Analytical Chemist to support GMP testing of pharmaceutical in-process, raw material, intermediate, API, and stability samples. The role also supports investigations of invalid results and method transfer activities. The successful candidate is expected to demonstrate strong attention to detail and excellent organizational skills. The position involves conducting and reviewing testing in accordance with approved methods, specifications, protocols, and compendial requirements; following GMP regulations, including 21 CFR Parts 210 and 211 and applicable ICH guidelines; participating in method transfer, qualification, and verification studies; and supporting OOS, OOT, and invalid-result investigations. The chemist will use analytical techniques such as NMR, GC, LC, ICP-OES, IR, RI, UV-Vis, conductivity, specific rotation, titration, and TGA, and will support reference-standard qualification and management as well as elemental-impurity and residual-solvent testing and review. This is a permanent, full-time position with overtime as needed. The work schedule is 6:00 a.m.–4:30 p.m., with a choice of Sunday through Wednesday or Wednesday through Saturday. Candidates within commuting distance of Albany, New York, are encouraged to apply. Compensation is $30.00–$39.00 per hour, based on education and related industry experience.
Requirements
- Bachelor’s degree in Chemistry, Pharmaceutical Sciences, Life Sciences, or a related field and 3 or more years of GMP/GLP testing experience; or a master’s degree in one of these fields and 1 or more years of industry GMP/GLP testing experience.
- At least 1 year of industry experience with Liquid Chromatography (LC), conductivity, and titration.
- Experience using at least two of the following techniques or instruments: NMR, GC, ICP-OES, IR, RI, UV-Vis, and TGA.
- Knowledge and in-depth understanding of GMPs, ICH, and 21 CFR guidelines.
- High attention to detail and excellent organizational skills.
Nice To Haves
- At least 1 year of GMP experience.
Responsibilities
- Conduct and review testing in accordance with approved methods, specifications, protocols, and compendial requirements.
- Follow GMP regulations, including 21 CFR Parts 210 and 211, and applicable ICH guidelines.
- Test pharmaceutical in-process, raw material, intermediate, API, and stability samples.
- Participate in method transfer, qualification, and verification studies.
- Support investigations for OOS, OOT, and invalid results.
- Use analytical techniques including NMR, GC, LC, ICP-OES, IR, RI, UV-Vis, conductivity, specific rotation, titration, and TGA.
- Support reference-standard qualification and management.
- Perform and review elemental-impurity and residual-solvent testing.
Benefits
- Comprehensive medical coverage.
- Dental and vision options.
- Life and disability insurance.
- 401(k) with company match.
- Paid vacation and holidays.
- Eligibility for a yearly goal-based bonus and merit-based increases.
- Competitive benefits package and work-life balance.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
