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Piramal Pharma Limited

Executive-Quality Control

Piramal Pharma Limited
Early Applicant
  • 3 months ago
  • Be among the first 50 applicants
Exp: 0-2 Years
Mumbai, India
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Job Description

  1. To prepare, review and update SOP, Specification, Method of analysis, report and protocol.
  2. To review IQ, OQ, PQ of new instrument.
  3. To review the documents such as inprocess, intermediate, cleaning validation, water reports as per cGMP.
  4. To attend the trouble shooting of QC instruments and to co-ordinate with the authorized supplier for support if any.
  5. To check the training program are conducted as per training schedule.
  6. To maintain, execute and update calibration and validation schedule of all QC instrument.
  7. To ensure the cGLP practices are followed in QC department.
  8. Handling change control related documentation in QC department.
  9. Monitoring the procedures related to Laboratory management is followed as per SOP.
  10. Involved in investigations like Deviation, OOS, OOT etc.
  11. Ensuring completion of investigations with documentation within the specified timeframe.
  12. Ensuring that the CAPA implementation and effectiveness review in QC department.

More Info

Industry:Other

Function:Pharmaceuticals

Job Type:Permanent Job

Skills Required

OQ
Laboratory Management
Cgmp
IQ
specification
Capa
Change Control
Sop
Oos
Calibration
Validation
Deviation

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Date Posted: 09/08/2024

Job ID: 88083747

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