- Ensure compliance with GMP, GLP, and SOP guidelines.
- Monitor and maintain quality assurance activities in the pharmaceutical manufacturing unit.
- Review and maintain batch manufacturing records (BMR) and batch packing records (BPR).
- Handle documentation and ensure proper record maintenance.
- Conduct in-process quality checks and monitor manufacturing activities.
- Ensure compliance with regulatory requirements and quality standards.
- Coordinate with Production and QC departments.
- Support audits, inspections, and deviation investigations.
Candidate Requirements:
- Relevant experience in QA in the pharmaceutical industry.
- Positive knowledge of GMP, SOPs, and pharmaceutical documentation.
- Strong attention to detail and quality standards.
- Must be available for immediate joining.
Interview Process: Face-to-Face Interview Only.
Important: Candidates interested in online, virtual, or telephone interviews should not apply.
Interested candidates can share their updated CV or contact us directly.