Executive Manufacturing QMS and compliance Injectable

Amneal Pharmaceuticals


Date: 2 weeks ago
City: Ahmedabad, Gujarat
Contract type: Full time
Job Description

  • Responsible for preparation & review of the master documents of sterile manufacturing for parenteral facility.
  • Responsible for preparation and review of protocols and reports based on the requirements.
  • Responsible for document management and preparation like BMR’s, BPR’s, master SOP’s etc.
  • Responsible for the handling of change control, deviations, CAPA, investigation etc.
  • Responsible to give training to all the subordinates, technicians and operators of the department.
  • Responsible for Audit and compliance on manufacturing shopfloor.
  • Knowledge of kaizen and continuous improvements.

Qualifications

Qualification: B.Pharm/M.Pharm candidate with minimum 3-5 years experience in manufacturing QMS/Process review/Compliance.

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