Job Title: Executive - Quality Assurance, Pharma
Educational QualificationB. Pharm / M. Pharm from a reputed university
Experience3 to 6 years of similar experience in a regulatory-approved OSD manufacturing large unit.
Job Responsibilities & Accountabilities:
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
What We're Looking For:3 to 6 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
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