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About the Role
Supplier Quality Management:
- Drafting of Annual Monitoring and Certification report for incoming materials
- Drafting / Negotiation (if applicable) and Archival of Quality Assurance Agreement with Suppliers/Service providers
- Evaluation and Management of Supplier Change Notifications (SCN) and Initiation of change record for the applicable SCN
- Drafting and Evaluation of Supplier’s incoming materials Specification
- Performing Quality Risk Assessment (QRA) for existing and new Suppliers / Service providers
- Management of Supplier/ Material qualification and supplier related documentations
- Preparation of regulatory statement for materials and finished products
- Management Quality records, Support the Service Delivery team (SDT) with quality topics and 3rd PAP Management in TPRM (Third Party Risk Management) tool
- Co-ordination with stakeholders in SIM (Supplier Information Management) approval process for Quality deliverables
- Evaluation of Change control tasks related to supplier quality management
- Audit preparation support and CAPA Management
- End to end deliverables for supplier quality management activities as per the delegated task from the business partner.
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Accessibility and accommodation
Novartis is committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to diversityandincl.india@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.
