Senior Analyst, Quality Control
Core
Conduct chemical and physical laboratory tests on excipients, raw materials, intermediates, and final products to ensure compliance with standards and production targets.
Role type
Senior IC Quality Control Analyst (Pharmaceutical)
Builds
Final Certificates of Analysis (CoA), validated analytical methods, and compliant test data for pharmaceutical products.
Domain
Pharmaceutical manufacturing / Quality Control
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
HPLC, Dissolution testing, GC, FTIR, Electro Chemistry (DME), UV/Vis, Wet chemistry, cGMP compliance, USP knowledge, Laboratory troubleshooting, Data integrity management, Method validation, Instrument qualification (URS/IQ/OQ/PQ), Team coaching, Process improvement
Preferred skills
Experience in pharmaceutical manufacturing facility, Expertise in analytical instrumentation, Strong presentation skills for upper management, 3rd level qualification in Science
Technologies
LIMS, HPLC, GC, FTIR, UV/Vis, DME
Responsibilities
Conduct and analyze chemical/physical tests for raw materials and final products; Verify testing records and documentation; Compile datapacks and generate Final CoA; Report deviations and OOS issues; Coach team members on test execution; Improve team efficiency and adherence to test schedules; Author cGMP-compliant documents (investigations, deviations, method validations); Maintain data integrity per FDA/GLP/QSR/cGMP regulations.
Seniority
Senior, hands-on IC with team leadership responsibilities