Executive - Quality Control (Formulation)

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:
  1. Responsible for Overall management of Quality Control Laboratory and compliance to applicable standards.
  2. To approve or reject, as he sees fit, raw materials, packing materials, semi finished product and finished products as per agreed/approved Specification.
  3. To review and approve analytical reports, validation protocols, calibration reports, environmental monitoring planner and other documents of microbiology laboratory.
  4. Preparation and review of department SOP;s related to Quality control and microbiology laboratories.
  5. To ensure instruments are calibrated timely and review of their records.
  6. To ensure analyst are validated for required testing.
  7. Procurement and Management of Reference and working standards
  8. To participate in the Investigation of complaints related to Quality of product.
  9. To participate in the Management review of product Quality, QMS and continue improvement.
  10. To ensure timely and effective communication with the management to raise Quality issue.
  11. Review of analytical data.
  12. To carry out investigation in case of any OOs, incidence, deviation.
  13. To involve and to participate in "Internal audit" Activities.
  14. To ensure followance of data back up procedure.
  15. To involve and to participate in cleaning validation, method validation and process validation activities.
  16. To monitor & approve water analysis trend charts.
Company Profile
Formulation

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