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Zentiva

Executive QA Documentation

India / Ankleshwar

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hirly's read of this role

Seniority
Mid level
Country
IN
Work mode
On-site / unstated
First seen by hirly
3 Oct 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

Position Title: Executive QA Documentation

Qualifications & Experience

Educational Qualification

Bachelor’s or master’s degree in pharmacy, Pharmaceutical Sciences, Life Sciences, or a related discipline.

Experience

1–5 years of relevant experience in Pharma Quality Assurance / Documentation

Skills & Competencies

  • Strong knowledge of cGMP, GDP, and Quality Systems
  • Hands-on experience with batch documentation and document control systems
  • Good understanding of APQR preparation and regulatory expectations
  • Strong analytical, organizational, and coordination skills
  • Effective communication and cross-functional collaboration abilities
  • Attention to detail and commitment to data integrity

Key Responsibilities

Review of Master Documents

  • Review and maintain Master Batch Manufacturing Records and Master Batch Packing Records to ensure accuracy, regulatory compliance, and alignment with approved specifications and process related changes.
  • Coordinate with Production, QC, and Regulatory Affairs for timely updates and approvals.

Annual Product Quality Review (APQR)

  • Prepare, compile, and review Annual Product Quality Reviews (APQRs) in line with regulatory expectations.
  • Support identification of improvement opportunities and follow-up of CAPAs arising from APQR findings.

cGMP Training Coordination

  • Coordinate and monitor cGMP and quality-related training programs for site personnel.
  • Maintain trainingschedules, records, and effectiveness assessments.

Archival & Records Retention

  • Manage the archival room and document storage systems for controlled and historical GMP documents.
  • Ensure secure storage, easy retrieval, retention compliance, and protection against unauthorized access or damage.
  • Support audits and inspections by ensuring availability of archived records.
Original posting on Zentiva's site ↗

Listed on hirly, a job board. hirly is not the employer: Zentiva is hiring for this role.

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