Executed GMP-compliant physicochemical and analytical testing of pharmaceutical raw materials, in-process samples, and finished dosage forms, ensuring adherence to approved SOPs and pharmacopeial standards.
Generated, reviewed, and controlled quality-critical laboratory documentation, including analytical worksheets, batch manufacturing records, certificates of analysis (CoA), and deviation reports, maintaining 100% data integrity and traceability for NAFDAC compliance.
Supported Quality Assurance activities by participating in OOS/OOT investigations, change control documentation, and corrective and preventive actions (CAPA), enhancing process reliability and regulatory standing.
Operated and maintained advanced laboratory equipment, ensuring accurate and reliable results for critical quality control analyses.