QC Analytical Chemist
About The Position
Eurofins 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, and requires strong attention to detail and organizational skills. The chemist conducts and reviews testing under approved methods, specifications, protocols, and compendial requirements. The position uses a range of analytical techniques and supports reference-standard management, elemental impurity and residual-solvent testing, method transfer, qualification and verification studies, and investigations into OOS, OOT, and invalid results. This is a permanent, full-time position with overtime as needed. The schedule is 6:00 a.m.–4:30 p.m., four 10-hour days per week (40 hours total), working either Sunday–Wednesday or Wednesday–Saturday.
Requirements
- Bachelor’s degree in Chemistry, Pharmaceutical Sciences, Life Sciences, or a related field and at least one year of GMP/GLP testing experience; or a master’s degree in one of these fields and at least six months of industry GMP/GLP testing experience.
- At least one year of industry experience with Liquid Chromatography (LC), conductivity, and titration.
- Proven experience using at least two of the following techniques or instruments: NMR, GC, ICP-OES, IR, RI, UV-Vis, or TGA.
- Knowledge and in-depth understanding of GMPs, ICH, and 21 CFR guidelines.
- Authorization to work indefinitely in the United States without restriction or sponsorship.
Nice To Haves
- At least one year of GMP experience.
Responsibilities
- Conduct and review testing in accordance with approved methods, specifications, protocols, and compendial requirements.
- Follow GMP protocols and applicable requirements, including 21 CFR Parts 210 and 211 and ICH guidelines.
- Test pharmaceutical in-process, raw material, intermediate, API, and stability samples.
- Participate in method transfer, qualification, and verification studies.
- Support investigations of OOS, OOT, and invalid results.
- Use analytical techniques including NMR, GC, LC, ICP-OES, IR, RI, UV-Vis, conductivity, specific rotation, titration, and TGA.
- Qualify and manage reference standards.
- 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 yearly goal-based bonus and merit-based increases.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
