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Job Description
Department: QA(QMS)
Designation: Executive
Experience: 5-6 years
Industry: Pharmaceutical Manufacturing
Job Responsibility
- Initiate and perform the process validation, and qualification of equipments 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 SOPs 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 datas for yearly and quarterly compilation for QMS
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Skills
AuditCapaChange ControlCleaning ValidationGmpInvestigationOosOotPqrProcess ValidationQaQcQmsIf an employer asks you to pay any kind of fee, please notify us immediately. Jobaaj does not charge any fee from the applicants and we do not allow other companies also to do so.
Important dates & deadlines?
Application Deadline
23 Jun 25, 11:23 AM IST
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