We are seeking a detail-oriented QA Officer to join our pharmaceutical manufacturing team. You will ensure our production processes strictly comply with GMP guidelines, manage quality documentation, and uphold the highest standards of drug safety and efficacy.
Key Responsibilities:
- Maintain and update Standard Operating Procedures (SOPs) and batch records.
- Perform line clearances and in-process quality checks.
- Investigate manufacturing deviations and implement CAPA.
- Assist in internal self-inspections and external regulatory audits.
- Ensure strict adherence to data integrity (ALCOA+) principles.