QC Analyst, First Shift
Core
Conduct routine and non-routine analysis of in-process testing and finished products using UV-Vis, HPLC, LC-MS, and other analytical techniques to ensure product stability and compliance.
Role type
Quality Control Analyst (Analytical Chemistry)
Builds
Analytical data and compliance documentation for biochemical and chemical products
Domain
Life Sciences / Pharmaceutical Manufacturing
Required skills
UV-Vis spectroscopy, HPLC operation, LC-MS operation, IC solution preparation, sample preparation, data compilation, equipment calibration, SOP revision, investigation reporting
Preferred skills
FDA regulatory knowledge, post-graduate certification, license
Technologies
UV-Vis, HPLC, LC-MS, IC
Responsibilities
Conduct routine and non-routine analysis of in-process testing according to standard operating procedures; Perform biochemical and/or chemical analyses of products, in-process items, and finished products; Calibrate and maintain lab equipment; Compile data for documentation of test procedures; Review data for compliance with specifications and report abnormalities; Revise and update standard operating procedures as needed; Participate in the preparation of investigations, summaries, and reports
Seniority
Mid-level, hands-on IC