Company: ZIM Laboratories Ltd

Department: QA(QMS)

Designation: Executive

Experience: 5-6 years

Industry: Pharmaceutical Manufacturing


Job Responsibility:


  1. Initiate and perform the process validation, and qualification of equipment’s and instruments.
  2. Initiate and perform Product Quality Review.(PQR)
  3. Handling of OOS, OOT, Deviation, CAPA and its root cause investigation for Market Complaint.
  4. Review of balances calibrationas per GLP requirement and review of Specifications for FG.
  5. Review of logbook of QMS & manufacturing, packing, WH, QC, housekeeping department.6Preparationof new SOP’s for QMS activities and investigation of Incident, Deviation & OOS.
  6. Responsible for performing self-inspection of different sections.
  7. Initiate cleaning validation as per regulatory requirement and review its protocol and reports(Cleaning Validation).
  8. Change control Management as per life cycle of process and audit compliances.
  9. Responsible to provide training as and when required as per TNI schedule.
  10. Responsible for TQM system with GDP and GMP implementation.
  11. Responsible for decontamination and hold time study.
  12. Responsible for trending of data’s for yearly and quarterly compilation for QMS

If Interested Share your Resume at careers@zimlab.in.