Executive - Quality Control (Formulation)
3 Nos.
68653
Full Time
2.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 4.00 LPA
Production / Quality / Maintenance
Pharma/Biotech/Clinical Research
Job Description:
- Responsible for Overall management of Quality Control Laboratory and compliance to applicable standards.
- To approve or reject, as he sees fit, raw materials, packing materials, semi finished product and finished products as per agreed/approved Specification.
- To review and approve analytical reports, validation protocols, calibration reports, environmental monitoring planner and other documents of microbiology laboratory.
- Preparation and review of department SOP;s related to Quality control and microbiology laboratories.
- To ensure instruments are calibrated timely and review of their records.
- To ensure analyst are validated for required testing.
- Procurement and Management of Reference and working standards
- To participate in the Investigation of complaints related to Quality of product.
- To participate in the Management review of product Quality, QMS and continue improvement.
- To ensure timely and effective communication with the management to raise Quality issue.
- Review of analytical data.
- To carry out investigation in case of any OOs, incidence, deviation.
- To involve and to participate in "Internal audit" Activities.
- To ensure followance of data back up procedure.
- To involve and to participate in cleaning validation, method validation and process validation activities.
- To monitor & approve water analysis trend charts.
Key Skills :
Company Profile
Formulation
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