Job Description
To responsible for preparation and maintain cGMP, WHO documents.
To identify and address areas of non conformance and take appropriate corrective and preventive actions, further control non conformance till adequate actions are taken up.
Conduct and review Internal Quality Audits.
Line clearance at various manufacturing stages.
Issuance and verify of batch records.
Checking of master formula records and entered in software.
To investigate out of specification results or failure investigation related to testing or manufacturing etc.
SOP preparation, verification and control monitoring, issuance as well as retrieval.
Monitoring of process validation activity and raw data compilation. To prepare or verify the final report of Process Validation.
Handling and control monitoring over all controlled documents issuance and retrieval.
To handle and investigate deviations.
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