Senior SAP Master Data Coordinator

The actual location of this job is in Stein, AG, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.Join our dynamic and growing Drug Product Services (DPS) team and help shape the future of patient treatment. We're looking for a Senior ERP Process/ Master Data Specialist to support an exciting new sterile drug product facility in Stein —managing key data processes across our site in Stein and two additional locations. Be part of a collaborative team driving innovation through precise data management.What you'll get: An agile career and dynamic working culture An inclusive and ethical workplace Compensation programs that recognize high performance Along with competitive salaries, you'll find a wide range of lifestyle, family and leisure benefits available. The full list of our local benefits can be also found on assetstream.aspxWhat you'll do: Autonomous owner of the Master Data Setup in SAP R3 for several filling lines with global and local support in a fast growing environment Coordination of activities between various stakeholders involved in the new material creation process (e.g. external suppliers, Quality, MSAT, other sites etc.) Design and modification of BOMs, Recipes, resources, COA Profiles, Inspection Plans and Inspection Characteristics in SAP Actively improve processes and ensure SOPs related to new part set-up, BOM, recipe creations are up to date and usable Creation and maintenance of part codes in SAP (Material Master) In charge of changes required within the SAP system Independent design, preparation and writing of master data governance documents and process descriptions Actively tracking master data KPIs and ensuring corrective actionsWhat we're looking for: Strong Master Data (Material and Production) experience in SAP R3 or S4 Hana and MS Office Significant working experience in Supply Chain in a Manufacturing Site (e.g. in Work Preparation Department "AVOR") Work experience in the pharmaceutical industry in a GMP environment is a must Certification in APICS and/or CPIM would be a plus Capable to adapt and act in a project environment and fast changing business. You challenge the status quo and enjoy looking for opportunities to make improvements. Fluency English as well as fluency in German are a must Conceptual and strategic thinking mindset to be able to create and implement governance documents (e.g. work instructions, SOP)About LonzaAt Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.Ready to shape the future of life sciences? Apply now.