Posted:1 week ago|
Platform:
On-site
Full Time
To prepare and review Validation Master Plan (VMP, PVMP, CVMP, QMP). To follow the validation master plan.
· To prepare and review Validation Documents and execution as per protocol.
· Handling and storage of all quality document like BMR, BPR, log book, Protocol, Report and SOP throughout life cycle.
· To prepare and review standard operating procedures (SOP's) and procedures related to validation.
· Preparation and review of PPQ and cleaning validation protocol and summary reports.
· Monitoring of PPQ and cleaning validation activities.
· Coordination with cross functional team to perform validation activity.
· Addressing any deviation identified during validation activity.
· To participate in investigation.
· To support in change management, deviations, CAPA and all other quality management systems as and when required.
BDR Pharmaceuticals
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