Assistant Manager-CQA

Assistant Manager-CQA

work outline iconFresherrupess outline iconNot disclosed time outline iconFull Time

Sanzyme Ltd

time outline iconMedchal Malkajgiri, Telangana, India

Posted on 31-07-2025

1 Vacancy

Description

  • Review batch manufacturing and packing records (BMR/BPR).
  • Conduct in-process checks and line clearance during manufacturing.
  • Handle deviations, change controls, and CAPA documentation.
  • Perform audits – internal, vendor, and regulatory support.
  • Review and approve SOPs, protocols, and reports.
  • Coordinate with production, QC, and warehouse for compliance.
  • Monitor environmental conditions and perform quality risk assessments.
  • Ensure timely documentation and record-keeping.
  • Provide training to staff on quality systems and compliance.

Category

Pharmaceuticals

Functional Area

Pharma Quality Assurance (QA)

Key Skills

Good CommunicationAttention to DetailDecision MakingProblem Solving Skills

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