4 - 6 years
3 - 5 Lacs
Posted:6 hours ago|
Platform:
Work from Office
Full Time
plant.
Corrective and Preventive actions, OOS, OOT, Market complaints and Product recalls.
3. Responsible for investigations of different deviations, OOS, OOT, market complaints, product
recalls and Risk assessments.
4. Responsible for preparation of internal audit schedules and coordination and organization of
audit meetings and participation as Auditee / Auditor.
5. Responsible for facing all external audits in their domain.
6. Responsible for vendor qualification related activities and participate in vendor qualification.
7. Responsible for preparation of QA documents, APQRs and its annexures, Control, Review,
Issuance, retrieval and destruction of all plant documents in coordination with all the
departments.
8. Assisting and coordinating in internal & external audit related activities.
9. Responsible for implementation and maintenance of WHO-GMP within the facility.
10. Responsible for review of artworks and support to Regulatory affairs.
11. Responsible for Oracle / ERP related activities.
12. Any other activities assigned by the Reporting manager.
13. In his absence, other competent person assigned by competent authority will perform his
responsibilities under supervision of seniors.
MSc- Biotechnology/Micro biology, M pharmacy.
Preferring Females.
Preferring profiles from Injectables and formulations background only.
If any one is interested can send your updated resume to the mail id srividya.deram@globionindia.com
Best Regards,
Srividya,
Sr. HR Executive
Globion
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