Job
In this role, you will develop processes for Master Data Management and Artwork & Packaging, ensuring data quality and compliance with regulatory requirements in a global environment.
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Your role in the team
- 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.
- 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.
Our expectations of you
Education
- University degree in business, life sciences, engineering or a related field.
Qualifications
- 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.
- Structured and detail-oriented working style with strong analytical skills.
- Fluency in English; German would be a plus.
Experience
- 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).
- Experience working in cross-functional and international environments, ideally across Quality, Regulatory, Supply Chain or IT.
What we offer
- 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.
- Attraktive Lage mit guter Verkehrsanbindung, modernen Arbeitsplätzen und einem Firmenrestaurant.
- 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.
Benefits
Work-Life-Integration
Health, fitness & fun
Topics you will work on
Job locations
About your employer
SimCorp provides integrated, best-in-class investment management solutions to the world’s leading asset managers, fund managers, asset servicers, pension and insurance funds, wealth managers and sovereign wealth funds.
- 250+ Employees
- Established Company
- Hybrid, Onsite
- Banking, Finance, Insurance
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