Quality Control - Finished Goods - Officer
Quality Control - Finished Goods - Officer
Employer Active
Job Alert
You will be updated with latest job alerts via email
Share
Job Alert
You will be updated with latest job alerts via email
Job Description
Sample Analysis: Perform chemical and instrumental analysis (e.g. HPLC UV Dissolution Titration) of finished dosage forms like tablets capsules and injectables.
Pharmacopoeial Testing: Ensure compliance with USP BP IP Ph. Eur. standards during analytical procedures.
Documentation: Prepare and maintain test reports logbooks COAs and analytical worksheets following GMP and data integrity principles.
OOS/OOT Reporting: Identify and report out-of-specification (OOS) or out-of-trend (OOT) results deviations and participate in investigation and CAPA implementation.
Instrument Handling: Operate and maintain analytical instruments like HPLC UV and Dissolution Apparatus including calibration and troubleshooting.
Audit Readiness: Ensure records and reports are maintained in a manner that is audit-ready for inspections by USFDA MHRA WHO EU-GMP etc.
Coordination: Collaborate with QA Production and Warehouse for batch release support and timely documentation flow.
Required Experience:
Unclear Seniority
Employment Type
Full-Time
