QC Analytical Chemist - Group Leader
About The Position
Eurofins Professional Scientific Services is hiring a QC Analytical Chemist Group Leader to support and lead 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 leads a team of 3–5 individual contributors. The successful candidate will bring strong attention to detail and organizational skills. The position combines hands-on analytical testing and review with team leadership. Work is conducted in accordance with approved methods, specifications, protocols, compendial requirements, GMP regulations, and applicable ICH guidelines. The schedule is four 10-hour shifts per week, 40 hours total, on either Sunday–Wednesday or Wednesday–Saturday, with overtime as needed.
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, or TGA.
- Knowledge and in-depth understanding of GMPs, ICH, and 21 CFR guidelines.
- Prior leadership experience, such as training or mentoring, college committees, or industry leadership.
- Authorization to work in the United States indefinitely without restriction or sponsorship.
Nice To Haves
- At least 1 year of GMP experience.
- At least 1 year of successful leadership experience.
Responsibilities
- Conduct and review testing in accordance with approved methods, specifications, protocols, and compendial requirements.
- Follow GMP protocols and regulations, including 21 CFR Parts 210 and 211, and applicable ICH guidelines.
- Test pharmaceutical in-process, raw material, intermediate, API, stability, and other 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.
- Conduct and review elemental impurities and residual solvent testing.
- Lead, manage, and develop a team of chemists.
- Serve as a proactive point of contact for client and internal teams.
- Participate in new-hire interviews and onboarding as needed.
- Disseminate administrative communications and promote the company vision.
- Ensure high quality and efficiency standards in laboratory operations.
- Perform administrative tasks that support team-member growth and development.
- Balance technical work with team leadership responsibilities.
- Foster morale, collaboration, and teamwork within the group.
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
Mid Level
