Pharma Analytical Qms Exeutive
7 days ago
Prepare, review, and control SOPs and key documents.
- Review and control documents for analytical validation protocols and reports.
- Review instrument qualification, calibration, and maintenance data and reports.
- Participate in vendor and internal audits.
- Review computer system validation documents.
- Plan routine activities and report to QA Head or designee.
- Ensure Good Laboratory Practice in the laboratory.
- Conduct training and manage training-related documents.
- Have sound knowledge of regulatory requirements like ICH, USFDA, EU, Schedule L-1, and effective auditing skills.
- Knowledge and training in NABL and other ISO standards is preferable.
**Job Types**: Full-time, Permanent
Pay: ₹18,000.00 - ₹36,000.00 per month
**Benefits**:
- Health insurance
- Provident Fund
Schedule:
- Monday to Friday
Work Location: In person
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