Job Description:

  • Ensure timely revision/review and implementation of SOP, IOP’s, and EOP’s by keeping a track of documents to maintain the compliance status of IPD.
  • Review and assess change controls, deviations, and CAPA’s by coordinating with IPD to ensure effective implementation of approved changes/actions.
  • Review of CMC documents by coordinating with ADL to ensure Compliance with the regulatory requirements.
  • An Effective Execution of quality systems by coordinating with the ADL department to maintain overall compliance status to the laboratory.

Qualification: M.Sc/M.Pharma

Experience: 6-9 Yrs in QA and Computerized system validation &IT

Salary: Negotiable

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