Manager, Site SAP Data Maintenance and System Process

Working with Us
Challenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here uniquely interesting work happens every day in every department. From optimizing a production line to the latest breakthroughs in cell therapy this is work that transforms the lives of patients and the careers of those who do it. Youll get the chance to grow and thrive through opportunities uncommon in scale and scope alongside high-achieving teams. Take your career farther than you thought possible.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits services and programs that provide our employees with the resources to pursue their goals both at work and in their personal lives. Read more: Myers Squibb Netherlands

• Performs business impact assessment on changes to SAP system boundary systems and business processes and design Standard Operating Procedures and work instructions for system processes.
• Collaborate with peers Site IT and validation personnel to develop and prioritize testing of related system and associated boundary systems.
• Collaborate with peers Site IT engineering and validation personnel to support integration of boundary systems with SAP system in support of Site processes.
• Develop risk-based testing approach by understanding how to translate business requirements into data design to ensure a compliant efficient and effective system.
• Collaborate with IT and other site departments to develop and maintain site test scripts and other related testing documentation.
• Collaborate with IT and other site departments to manage testing execution related to the ERP system (i.e. development testing integration testing user acceptance testing regression testing).
• Understand site processes and the implementation within the global ERP and boundary systems (i.e. configuration and master data including but not limited to items recipes routings formulas process instructions and process variables).
• Develop and provide basic training to SAP S/4 HANA users.
• Collaborate with other site functions and IT to develop business requirements for business process improvements within global information systems.
• Coordinate with IT and other site departments to maintain supporting technologies that are compliant efficient effective and reliable.
• Act as site project coordinator as required for new systems enhancements to current systems and/or required regression or other testing coordinated at a global level.
• Coordinate documentation creation review and approval to support timelines for critical site milestones
• Coordinate and author site change control(s) as assigned to support implementation of and changes to business processes and above-site global systems (e.g. SAP S/4 EWM IBP Scheduling tool)
• Workcross-functionally collaborating across departments including manufacturing supply chain quality project teams and global functions.
• Lead assessment of changes to necessary SOPs work instructions and other controlled documents necessary to Master Data execution.
• Develops and implements master data performance measurement
• Collaborate within the Supply Chain department and with manufacturing quality control quality assurance IT and global master data management to determine business requirements for the design of master data
• Translate business requirements into a robust master data design which is compliant efficient and effective.
• Develop and execute cGMP change controls and change requests for master data changes
• Prepares and follows data templates and workflows to meet the requested timelines and makes the data entry in SAP EWM IBP Scheduling systems.
• Is CAPA action owner and change control action owner and must ensure that the proper actions are done in due time and according to the GxP guidelines and liaise with more global project timelines
• Ensures proper IT development; implements and executes the needed data tests/loads within the ERP system
• Plays an active role during UAT sessions for ERP improvement or org developments. He/she can be consulted during UAT script creation execution of tests related to master data production QC QA Scheduling and Warehouse functions/modules and can also participate as coordinator for these sessions.
• Maintain all master data field release process to meet end user requirements and to maintain compliant efficient and reliable batch records and supporting data.
• Collaborate with other stakeholders (global and site) to maintain and optimize product hierarchy while maintaining compliance and minimizing risk.
• Participates in project related to MDM activities as subject master expert and can lead or co-lead such project

• Bachelors degree in systems engineering or related field
• 12 years of experience in the biopharmaceutical and/or biotechnology industry with specific roles in systems master data management and/or data analytics
• Deep understanding in master data management ERP development and integrations with other Systems
• ERP/MRP Systems (i.e. SAP Oracle etc.) SAP preferred
• Intermediate knowledge of cGMP regulations
• Ability to provide on-call support in case of emergent issues
• Ability to interpret / write technical documents
• Experience with Interface projects SAP preferred
• Self-motivated proactive and able to work with minimal supervision