Major accountabilities:
1. Handling of Audit CAPA actions, Deviations and Investigations.
2. Preparation of annual audit plans
3. Monitoring and maintain of KQI's and KPI's.2.
4. Maintenace of Shrepoints and Repositories. ·
5. Responsible to update the information on SharePoint/ trackers, review the applicable documents for correctness and archival of necessary documents on SharePoint. ·
6. Provide Administrative support in preparation of Quality Management Review meeting slide deck & metrics reporting. ·
7. Preparation, approval, and management of QAA's.
8. Develop and maintain process SOPs, working procedures and process maps. ·
9. Provide support for GMP External Audits and inspection management activities (HA and Self Inspection Audits).
10. Maintain Approved supplier list for GxP vendors.
11. Preparation of UQAP (Unified Quality Audit Program), Audit preparation support and QARP (Quality assurance responsible Person) Role for audit CAPA Management.
Minimum Requirements:
M.Pharm/ equivalent from a reputed institute.
• Min 4-6 yr Experience in Quality Assurance, Regulatory or in the manufacturing of pharmaceutical drug substances or products/ Medical device.
• Basic awareness of GxP compliance requirements.
Work Experience:
Why Novartis: Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: http://www.novartis.com/about/strategy/people-and-culture
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