Assistant Manager

2 days ago


Ankleshwar, India Zentiva Group, a.s. Full time

Job Title: Sr. Executive / Assistant Manager – Quality Assurance, Pharma Educational Qualification B. Pharm / M. Pharm from a reputed university Experience 8 to 10 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: 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


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