QA Validation
3 months ago
Review of qualification documents URS, SIA, Risk assessment, DQ, IQ, OQ, and PQ.
Execution of qualification activities IQ, OQ, IOQ and PQ with support from vendor and user.
Preparation and review of performance verification protocols and reports.
Review of engineering related documents PM, AMC, and calibration schedules.
Preparation of equipment and area performance verification planners Yearly and Monthly.
Responsible for thePreparation VMP and updated yearly planner.
Review the all-department breakdowns and notifications & alarms
Review of SOPs related to Cross functional team related to equipment's
preparation and review of SOPs related to QA
Handling of Change controls and Deviations related to equipment and respective procedures
Conducting investigation in case of deviations during process related to equipment failure.
Effectiveness verification of CAPA implementation related to equipment.
Review of Drawings and layouts related to facility and their maintenance.
Note: We need two Manpower of around 2-3 years of experience in Pharma or Biotech industry.
**Job Types**: Full-time, Permanent
**Benefits**:
- Food provided
- Leave encashment
- Paid sick time
- Provident Fund
Schedule:
- Day shift
- Morning shift
- Rotational shift
**Education**:
- Bachelor's (preferred)
**Experience**:
- total work: 1 year (preferred)
Work Location: In person
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