This is a temporary contractor opportunity at Novartis
Novartis touches the lives of a tenth of the world’s population. Every role here, regardless of contract type, makes an impact on human life!
Ready to work with/through Magnit at Novartis? Please read on...
Main activities:
* Acts as TRD excipient portfolio manager
* Interacts and collaborates with internal and external stakeholders, customers and/or suppliers, according to specific area of responsibility.
* Maintains TRD excipient portfolio regarding supplier approval.
* Ensures change control management of excipient related matters notified by suppliers or triggered internally.
* Supports project teams in case of excipient-related request
* Handling of change actions and CAPAs, related to excipient involving multiple project users in TRD about supplier or product specifications.
* Guides project teams through new excipient implementation operations
* Acts as line unit representative to TRD Third Party QA organization with respect to TRD excipient portfolio and ensures that own deliverables are met.
* Acts as line unit representative and SME for interactions within TRD and with NTO excipient counterparts on local sites when needed.
* Supports PHAD Excipient Supply and Demand planning coordinators.
* Acts as key expert for new excipient/supplier implementation in TRD portfolio.
* Coordinates activities linked to transfer of excipient ownership from commercial site back to TRD in case of discontinuation.
* Maintains effective information channel with all involved parties. Communicates issues to involved partners.
* Ensures compliance to Novartis and other relevant regulations.
* Shows positive work ethics and influences others.
* Proposes and implements ideas for continuous process improvement also outside area of expertise/ organization.
* 1QEM: CAPA and Actions.
Experience/Professional requirements:
* Education: Degree in science, logistics & supply chain, business administration or equivalent with SAP knowledge.
* Min. 5 years of successful industry experience in the development of pharmaceutical industry (including GMP knowhow).
* Strong knowledge of relevant GMP regulations and policies.
* Expertise in supply chain (esp. material planning, logistics), business support and/or customer service roles, ideally in a pharmaceutical/chemical/biotechnical development or manufacturing environment.
* Interdisciplinary thinking and interest in collaboration with other functions.
* Excellent communication skills, organizational, planning and negotiation skills.
* Languages: Very good English (oral & written). German desired
Workload: 80%-100%
Role type: Onsite
Estimated start date: as soon as possible
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