Company: ZIM Laboratories Ltd
Department: QA(QMS)
Designation: Executive
Experience: 5-6 years
Industry: Pharmaceutical Manufacturing
Job Responsibility:
- Initiate and perform the process validation, and qualification of equipment’s and instruments.
- Initiate and perform Product Quality Review.(PQR)
- Handling of OOS, OOT, Deviation, CAPA and its root cause investigation for Market Complaint.
- Review of balances calibrationas per GLP requirement and review of Specifications for FG.
- Review of logbook of QMS & manufacturing, packing, WH, QC, housekeeping department.6Preparationof new SOP’s for QMS activities and investigation of Incident, Deviation & OOS.
- Responsible for performing self-inspection of different sections.
- Initiate cleaning validation as per regulatory requirement and review its protocol and reports(Cleaning Validation).
- Change control Management as per life cycle of process and audit compliances.
- Responsible to provide training as and when required as per TNI schedule.
- Responsible for TQM system with GDP and GMP implementation.
- Responsible for decontamination and hold time study.
- Responsible for trending of data’s for yearly and quarterly compilation for QMS
If Interested Share your Resume at careers@zimlab.in.