QC Analytical Chemist
Core
Conduct GMP-compliant analytical testing of pharmaceutical in-process, raw materials, intermediates, APIs, and stability samples, while supporting investigations of invalid results and method transfers.
Role type
QC Analytical Chemist
Builds
GMP-compliant test results and validated analytical methods for pharmaceutical clients
Domain
Pharmaceutical manufacturing and quality control
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
GMP/GLP testing, Liquid Chromatography (LC), Conductivity, Titration, Nuclear Magnetic Resonance (NMR), Gas Chromatography (GC), Inductively Coupled Plasma Optical Emission Spectroscopy (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; Reference standard qualification and management
Seniority
Entry to Mid-level, hands-on IC