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Job Description
Job Title: Sr. Executive / Assistant Manager Quality Assurance, Pharma
Educational Qualification
- B. Pharm / M. Pharm from a reputed university
- 8 to 10 years of similar experience in a regulatory-approved OSD manufacturing large unit.
We are looking for an experienced QA professional to join our team and lead Deviation & Complaint Investigations, along with core QMS activities.
Key Responsibilities
- Lead deviation and market complaint investigations, with timely CAPA execution
- Ensure effective implementation and tracking of CAPAs from deviations & complaints
- Review Batch Manufacturing & Packing Records, APQR, and SOPs
- Manage Change Controls, Validations/Qualifications, and QMS documentation
- Conduct regulatory gap assessments and support compliance plan execution
- Coordinate GMP training, documentation control, and audit readiness
- 810 years of QA experience in pharmaceutical manufacturing (formulations)
- Strong understanding of cGMP, investigation tools, and regulatory expectations (USFDA, MHRA)
- Skilled in QMS systems.
- Excellent documentation, analytical, and coordination skills
Skills
AuditApqrAssuranceCapaCgmpGmpInvestigationMhraQaQmsQms DocumentationQuality AssuranceSopsIf a job posting appears fraudulent, asks for payment, contains misleading information, or violates our guidelines, please report it immediately. Our team will review it promptly, Jobaaj does not charge any fee from the applicants.
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