About the Role
- Design and update Master Batch Records (MBRs) in alignment with global core processes.
- Provide MBR design and business process support to MES implementation projects and operating sites.
- Responsible for MES trainings and best practice sharing across Novartis sites.
- Enforce process standardization and harmonization across Novartis sites.
- Provide MES business configuration and master data support.
- Collaborate with the global and local teams in site fit-gap analysis for MES project preparation.
- Support the updates of standard operating procedures and global guidelines.
- Participate in MES communities of practices.
Requirements:
- Bachelor's degree in pharmaceuticals, chemistry or another relevant technical field.
- Fluent English. Other languages such as German and Slovenian are a plus.
- Experience in MBR design in MES PAS-X or MES Opstrakker.
- Experience in the pharmaceutical industry and knowledge of manufacturing processes.
- Good collaboration and interpernal skills as the role entails working across the Novartis sites.
Role Requirements
Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture
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Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards
