QC Analytical Chemist - 6pm-6am
Core
Conduct GMP-compliant analytical testing of pharmaceutical in-process, raw materials, intermediates, APIs, and stability samples, including method transfer and investigation of invalid results.
Role type
QC Analytical Chemist
Builds
Pharmaceutical quality control data and validated test results
Domain
Biopharmaceuticals / Analytical Chemistry
Required skills
GMP/GLP compliance, Liquid Chromatography (LC), Conductivity, Titration, Nuclear Magnetic Resonance (NMR), Gas Chromatography (GC), Inductively Coupled Plasma Optical Emission Spectrometry (ICP-OES), Infrared Spectroscopy (IR), Refractive Index (RI), Ultraviolet-Visible (UV-Vis), Thermogravimetric Analysis (TGA), elemental impurities testing, residual solvent testing
Preferred skills
Additional GMP experience
Technologies
NMR, GC, LC, ICP-OES, IR, RI, UV-Vis, Conductivity, Specific Rotation, Titration, TGA
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; Participate in method transfer, qualification, and verification studies; Support investigations for OOS, OOT, and invalid results; Utilize various analytical techniques including NMR, GC, LC, ICP-OES, IR, RI, UV-Vis, Conductivity, Specific Rotation, Titration, TGA; Reference standard qualification and management; Elemental impurities and residual solvent testing and review