About the Role

We are looking for an experienced and responsible QA Assistant Manager to support and manage Quality Assurance activities and ensure compliance with GMP, SOPs, quality systems, and applicable regulatory requirements.

Key Responsibilities

  • Support the QA Manager/Head in managing daily QA operations.
  • Ensure GMP, SOP, and quality system compliance across departments.
  • Review and monitor BMR, BPR, logbooks, and other manufacturing documents.
  • Handle and follow up on deviations, CAPA, change controls, and investigations.
  • Supervise IPQA activities, line clearance, and in-process compliance.
  • Review and maintain SOPs, quality records, and controlled documents.
  • Support internal, customer, and regulatory audits.
  • Coordinate with Production, QC, Warehouse, Engineering, and other departments.
  • Train and guide QA team members on GMP and documentation practices.
  • Prepare QA reports, trackers, and MIS for management review.

Requirements

  • Education: B.Pharm / M.Pharm / M.Sc. or relevant qualification
  • Experience: Minimum 4–6 years of experience in Pharmaceutical Quality Assurance
  • Strong knowledge of GMP, GDP, SOPs, and pharmaceutical documentation
  • Experience in handling BMR/BPR, deviations, CAPA, change control, and investigations
  • Knowledge of IPQA, line clearance, and in-process quality activities
  • Good leadership, communication, documentation, and team coordination skills

What We Offer

  • PF and ESIC benefits, as applicable
  • Paid leave and weekly off as per company policy
  • Performance-based annual increment
  • Training and professional development opportunities
  • Career growth and leadership opportunities
  • Safe and professional working environment
  • Other benefits as per company policy
Company
KDRS Group
Vacancies
27 Openings
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