Summary

Are you looking for an exciting opportunity to work with the latest technologies, collaborate with a top-performing team, and be surrounded by highly skilled professionals? We are seeking a talented and motivated associate to join our Novartis DDIT ITOT Global Manufacturing team.

Are you passionate about implementing and maintaining Manufacturing Execution Systems (MES) to streamline manufacturing processes? Join our team and play a pivotal role in our organization's success.

The Specialist Master Batch Record (MBR) Designer is responsible for supporting the sites in developing and implementing MBR's during the project deployments and site operations.

This role is essential in ensuring the smooth operation and continuous improvement of MES systems across all Novartis sites, contributing significantly to the organization's efficiency and compliance standards.

• 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.

• 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.