Zentiva Hiring B Pharm & M Pharm Professionals | Executive QA Documentation Role
Looking for a Pharma QA Job in pharmaceutical quality assurance and documentation? Zentiva is hiring an Executive QA Documentation professional for its Ankleshwar facility. This opportunity is ideal for pharmacy professionals seeking to build successful Zentiva Careers while gaining expertise in GMP compliance, APQR preparation, document control, and pharmaceutical quality systems.
- Job Title: Executive – QA Documentation
- Department: Quality Assurance
- Job Location: Ankleshwar, Gujarat, India
About the Company
Zentiva is a leading pharmaceutical company dedicated to providing high-quality and affordable medicines across global healthcare markets. With a strong focus on quality, compliance, and continuous improvement, Zentiva operates advanced manufacturing facilities that adhere to international regulatory standards. Professionals pursuing Zentiva Careers gain valuable exposure to pharmaceutical quality systems, regulatory compliance, and documentation excellence within a globally recognized pharmaceutical organization.
Job Description
The Executive QA Documentation will be responsible for managing GMP-controlled documents, reviewing master manufacturing and packing records, coordinating APQR activities, supporting cGMP training programs, and maintaining document archival systems. This Pharma QA Job provides hands-on exposure to pharmaceutical quality assurance, compliance management, documentation control, and quality systems while offering excellent growth opportunities through Zentiva Careers
Key Responsibilities
- Review Master Batch Manufacturing Records (MBMR).
- Review Master Batch Packing Records (MBPR).
- Coordinate document revisions and approvals.
- Maintain document control systems and GMP records.
- Prepare and review Annual Product Quality Reviews (APQR).
- Support CAPA implementation and follow-up activities.
- Identify product and process improvement opportunities.
- Coordinate cGMP and quality-related training programs.
- Maintain training records and effectiveness assessments.
- Support site-wide quality compliance activities.
- Manage archival and document retention systems.
- Ensure secure storage and retrieval of GMP records.
- Support audits and regulatory inspections through proper documentation management.
Eligibility Criteria
- Education: B. Pharm, M.Pharm, Pharmaceutical Sciences
- Experience: 1–5 years of experience in Pharmaceutical Quality Assurance or Documentation.
- Required Skills: cGMP, GDP, Quality Systems, Data Integrity, Batch Documentation, Document Control, APQR, Records Management, Analytical Skills, Coordination, Communication, Organization Skills
This Pharma QA Job at Zentiva offers an excellent opportunity for professionals looking to strengthen their expertise in pharmaceutical quality assurance, GMP compliance, and documentation management. Candidates interested in advancing their careers through Zentiva Careers can gain valuable experience in quality systems, APQR preparation, and regulatory compliance while contributing to pharmaceutical excellence.
