Executive Pharma QA at Zentiva – Apply Online Now!
Step into a role where your expertise in pharmaceutical quality assurance directly supports global healthcare. Zentiva is looking for a Quality Assurance Executive to join our growing team in Ankleshwar, India. This opportunity is ideal for professionals with a strong background in GMP, documentation, and quality systems who are ready to contribute to the manufacturing of reliable, affordable medicines.
About Zentiva
Zentiva is a manufacturer of quality, affordable medicines for patients in Europe and beyond. With over 4,700 employees and a network of manufacturing facilities – including flagship manufacturing facilities in Prague, Bucharest, and Ankleshvar – our goal is to become a leader in branded and generic medicines in Europe, better meeting people’s everyday healthcare needs. At Zentiva, we believe that healthcare should be a right, not a privilege. More than ever, people need better access to quality, affordable medicines and appropriate healthcare. In partnership with doctors, pharmacists, wholesalers, regulators, and governments, we deliver the everyday solutions we all rely on.
Executive – Quality Assurance Job Details:
Job Post: Executive – Quality Assurance, Pharma
Location: India / Ankleshwar
Time Type: Full-time
Posted on: Published yesterday
Job Requisition ID: R2467843
Educational Qualification
B. Pharm / M. Pharm from a reputed university
Experience for Executive – Quality Assurance Job
2 to 5 years of similar experience in regulatory-approved OSD manufacturing large units.
Quality Management/Continuous Improvement
- Line Clearance and shop floor compliance
- In-process checks and sampling activity
- Assisting in the Complaint Investigation system at the site
- Assisting in Qualification and validation system, change control system, deviations
- Preparing & reviewing the Annual Product Quality Review
- Review of Batch Manufacturing & Packing Records
- Coordination of cGMP Training activities
Documentation Control
- Preparation of quality system SOPs
- Controlled distribution and archival of documents & records
- Master document control
- Management of the archive room
- Issuance of batch records, ATR, logbooks, and controlled formats
Assuring the Quality of Products by
- In-process controls
- Review of Executed Batch Manufacturing & Packing Records
- Ensuring implementation of Corrective actions/Preventive actions proposed in Deviations and Customer complaints
- Ensuring the effectiveness review of the implemented CAPA
- Review of batch records & analytical testing records
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