- To maintain track of all documents across the company.
- Review and follow up of documentation such as change control, deviation, Internal audit, Market complaint, APR
- Review of batch manufacturing record preparation of SOPs, Specification, test method and raw data protocol.
- ISO documentation.
Desired Candidate Profile :
M.Sc. (Chemistry) with 5 - 8 yrs Experience in Quality Assurance of API /bulk drug manufacturing facility.
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