Assistant Manager-CQA
Sanzyme Ltd
Medchal 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
Aggregated job.
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