Quality Control Documents in Pharmaceutical
2 months ago
Experience - 6 Yrs in Pharmaceutical Quality **Documentation**
**Salary - 30,000 to 35,000 Per Month**
- Monitor the testing and Release of Raw materials, In process and finish products in stipulated time.
Manage all quality documentation.
- Sample management of RM/PM/in process/FP.
- Monitor stability sample testing and preparation of stability report.
- Preparation of AMV protocol and report
- Responsible for routine release of swab and rinse water analysis
- Responsible for HPLC operations
- Responsible for preparation and implementation of qualification/calibration schedule.
- Responsible to prepare/update STS/STP/worksheet/COA of RM, PM, In process, FP..
- Preparation and maintain preventative maintenance (AMC) and calibration calendar.
- Maintain laboratory in good condition to face the regulatory audits.
- Responsible for Calibrations of all QC instruments.
- Responsible to follow related SOP’s
- Job Allocation of QC persons.
- Initiation and closing of QMS documents like Out Of Specification, Change Control, Deviations, CAPA, Incidence report, etc.
- Facing the Internal/External audits.
- Responsible for Analyst qualification and training.
- Responsible for completion of log books.
- Procurement of Chemicals/Reagents/Reference standard/impurity and maintain the inventory.
- Responsible for timely review the raw data generated in Quality Control Laboratory.
**Salary**: ₹30,000.00 - ₹35,000.00 per month
**Benefits**:
- Provident Fund
Schedule:
- Day shift
Supplemental pay types:
- Performance bonus
**Experience**:
- Pharma Quality Document: 6 years (preferred)
Work Location: In person
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