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Assistant Manager - Quality Assurance, Pharma
Zentiva Group, a.s.ankleshwar, India1 day ago
Job description8 to 10 years of similar experience in a regulatory-approved OSD manufacturing large unit. 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 8–10 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
Job Title : Sr. Executive / Assistant Manager – Quality Assurance, Pharma
Educational Qualification
- B. Pharm / M. Pharm from a reputed university
Experience
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 :
What We’re Looking For :
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Quality Assurance Manager • ankleshwar, India
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