Key Responsibilities
Responsible for framing, controlling and issuance of SOPS and guidelines
To ensure the issuance, archival and retrieval of documents
Taking care of internal quality audit & documentation
To record the key, live observations during the actual audit
Publishing reports, observations and the corrective as well as preventive actions
- To ensure the proper archival/storage of final compounds and intermediates as per
the defined process
Key Requirements
- Good understanding of CGMP, GLP, GDP &
Knowledge of analytical instruments like
HPLC, LCMS etc. will be an added advantage.
Experience
0-2 years
Qualification
B. Pharma/M.Pharma
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