Company: Ajanta Pharma Ltd
Post: Officer or Sr. Officer: QA
Experience: 5 to 7 yrs
Qualification: B.Pharm. / M.Sc.
Job description:
- Responsible for fulfillment of regulatory requirements of Drug Regulatory Affairs (DRA) department.
- Review and online maintenance of cGMP and analytical documents of quality control.
- Document control (Issuance, retrieval, storage and destruction).
- Review and investigation of Out of Specification (OOS) investigation.
- Review of specification, Standard Test Procedure (STP) & General Test Procedure (GTP).
- Review and maintenance of deviation, incidence, corrective and preventive actions, non- conformance and change control.
- To ensure the integrity of data.
- Review of analytical method validation / verification of documents.
- Review of cleaning validation documents.
- Review of technology transfer documents.
- Placing of portable data logger in to the consignment, preparation of report and trending.
- The candidate should have exposure of Quality Control department.
Job Location
Ajanta Pharma Ltd.
Paithan MIDC, Paithan
Dist – Aurangabad (Maharashtra)
Virtual interview shall be planned for the same.
CV can be sent at:
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