Quality Control Analyst - Second Shift
Core
Conduct routine and non-routine analyses of raw materials, in-process samples, and finished products to ensure compliance with CGMP and regulatory requirements.
Role type
Quality Control Analyst
Builds
Analytical data and test reports for clinical and commercial products
Domain
Life sciences / Pharmaceutical manufacturing
Required skills
Analytical chemistry, HPLC/HPLC-MS, UV-Vis, Karl Fischer, pH measurement, Good Manufacturing Practices (CGMP), Good Documentation Practices (GDP), data review and compliance reporting
Preferred skills
CGMP/CDMO/pharmaceutical settings experience, FDA/international regulations knowledge (USP, JP, EP, ICH), Agilent instrumentation familiarity
Technologies
HPLC, HPLC-MS, UV-Vis, Karl Fischer, pH meters, Microsoft Excel, Microsoft Word
Responsibilities
Perform biochemical and chemical analyses on raw materials and final products, review data for specification compliance, collaborate with manufacturing and QC management, participate in laboratory equipment maintenance, support laboratory investigations
Seniority
Mid-level, individual contributor
