QC Analytical Chemist - Night Shift
Core
Conduct GMP-compliant analytical testing of pharmaceutical samples (in-process, raw materials, APIs, stability) and support method transfers and invalid result investigations.
Role type
QC Analytical Chemist
Builds
GMP-compliant test results and validated analytical methods for pharmaceutical clients
Domain
Pharmaceutical manufacturing and quality control
Required skills
GMP/GLP compliance, Liquid Chromatography (LC), Conductivity, Titration, Nuclear Magnetic Resonance (NMR), Gas Chromatography (GC), ICP-OES, Infrared Spectroscopy (IR), UV-Vis, TGA, elemental impurities testing, residual solvent testing, OOS/OOT investigation
Preferred skills
Additional GMP experience
Technologies
NMR, GC, LC, ICP-OES, IR, RI, UV-Vis, Conductivity, TGA, Titration
Responsibilities
Conduct testing and review in accordance with approved methods, specifications, protocols, and compendial requirements; Follow protocols for GMP regulations, including 21 CFR Parts 210 and 211, and applicable ICH guidelines; Testing of pharmaceutical samples including in-process, raw materials, intermediates, API, stability, and more; Participate in method transfer, qualification, and verification studies; Support investigations for OOS, OOT, and invalid results; Reference standard qualification and management; Elemental impurities and residual solvent testing and review
