Senior QC Analytical Chemist - Group Leader

Eurofins USA PSS Insourcing Solutions•Albany, NY

About The Position

Eurofins Professional Scientific Services is hiring a Senior 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 laboratory work with team leadership. The group leader oversees quality and efficiency in laboratory operations, serves as a point of contact for client and internal teams, and supports the professional development and collaboration of team members. This is a permanent, full-time position with overtime as needed. Work is scheduled from 6:00 a.m. to 4:30 p.m., with either a Sunday–Wednesday or Wednesday–Saturday schedule. Candidates within commuting distance of Albany, New York, are encouraged to apply.

Requirements

Bachelor's degree in Chemistry, Pharmaceutical Sciences, Life Sciences, or a related field and 5 or more years of GMP/GLP testing experience; alternatively, a master's degree in one of these fields and 3 or more years of industry GMP/GLP testing experience.
At least 3 years 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.
In-depth knowledge and understanding of GMPs, ICH, and 21 CFR guidelines.
At least 1 year of prior leadership experience.
High attention to detail and excellent organizational skills.

Nice To Haves

At least 2 years of successful leadership experience.

Responsibilities

Conduct and review testing in accordance with approved methods, specifications, protocols, and compendial requirements.
Follow GMP protocols, 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.
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 and effective point of contact for client and internal teams.
Participate in new-hire interviews and onboarding as needed.
Disseminate administrative communications and promote company vision.
Ensure laboratory operations meet high quality and efficiency standards.
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.