QC Analytical Chemist - Night Shift

Eurofins•Albany, NY

7h•$24 - $31

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 position conducts and reviews testing under approved methods, specifications, protocols, and compendial requirements. It follows GMP regulations, including 21 CFR Parts 210 and 211, and applicable ICH guidelines. The chemist uses a variety of analytical techniques and supports method transfer, qualification, and verification studies, investigations, reference-standard management, and elemental impurities and residual-solvent testing and review. The schedule is 10:00 PM to 8:30 AM, four 10-hour shifts per week for 40 hours total, on either Sunday through Wednesday or Wednesday through Saturday. Overtime may be needed. Compensation is $24.25–$31.25 per hour, based on education and related experience.

Requirements

Bachelor’s degree in Chemistry, Pharmaceutical Sciences, Life Sciences, or a related field, with at least one year of GMP/GLP testing experience; or a master’s degree in one of these fields, with 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.
High attention to detail and excellent organizational skills.

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 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 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.