As our Business Process Owner – Master Data & Artwork Coordination (m/f/d) you are responsible for the governance, design and continuous development of global master data- as well as artwork- and packaging processes in a regulated pharmaceutical environment. Acting as global process authority, you ensure data quality, compliance and standardized processes across the product lifecycle. YOUR CONTRIBUTION Process Ownership & Governance: Own global master data - as well as artwork - and packaging processes, defining standards, workflows and KPIs, and ensuring consistent execution across regions Master Data Management: Ensure accurate, compliant and consistent master data across all relevant SAP objects throughout the product lifecycle Artwork & Packaging Process Management: Govern end-to-end artwork and packaging processes, including creation, approval, version control and change management in line with regulatory requirements System & Digital Enablement: Translate business requirements into system - and process solutions within SAP-based environments and support system enhancements and implementations Compliance & Regulatory Alignment: Ensure adherence to GxP/GMP, data integrity, serialization and audit requirements across all master data - and artwork processes Performance & Continuous Improvement: Monitor KPIs (e.g. data quality, processing times, artwork lead times) and initiate improvements to enhance efficiency and standardization Cross-functional Collaboration: Work closely with Quality, Regulatory, Supply Chain, IT and external partners to ensure alignment across processes and systems Change Management & Training: Support the rollout of new processes and systems through stakeholder communication, training and process adoption YOUR PROFILE University degree in business, life sciences, engineering or a related field Relevant experience in master data management, process management or related roles within the pharmaceutical or regulated environment Experience with SAP master data structures and processes (e.g. SAP ECC/S4 HANA, ideally MDG, PLM or related systems) Understanding of end-to-end master data and/or artwork and packaging processes across the product lifecycle Solid knowledge of GMP, GxP, data integrity and regulatory requirements Experience working in cross-functional and international environments, ideally across Quality, Regulatory, Supply Chain or IT Structured and detail-oriented working style with strong analytical skills Fluency in English; German would be a plus YOUR BENEFITS Individual career development in a purposeful job: you improve the quality of life of our patients! Hybrid work model that allows a good work-life balance Attractive location with good transport links, modern workplaces and a company restaurant Global family business with flat hierarchies and an open, respectful corporate culture Attractive remuneration with extensive social benefits Variety of employer-subsidized benefits such as WellPass, Germany ticket, Corporate Benefits and JobBike Find out more about our benefits here. ABOUT US Welcome to Merz Therapeutics, a leading pharmaceutical company that helps people with movement disorders, neurological diseases, liver diseases and other health conditions regain their quality of life. We are proud to be a family-owned and value-driven company that has been dedicated to serving the needs of our patients for 110 years and is now a global innovation leader with products in more than 90 countries. Our goal is to use our products to improve treatment outcomes for patients around the world, thereby reducing the burden of suffering for affected people and their surroundings. Our dedication and commitment to relentless research and development is to ensure that unmet patient needs are identified and appropriate treatments are provided. Therefore, become part of our international and motivated Merz Therapeutics family now and help us achieve our goal: "BETTER OUTCOMES FOR MORE PATIENTS" For more information, visit https://www.merztherapeutics.com/ .