Global Product Owner (m/f/d)– MLR (Medical Legal Regulatory)
Machine translation — original language: German.Show original
Introduction/About us
As Global Product Owner (m/f/d) for MLR, you will be responsible for the product vision, roadmap, delivery, and continuous improvement of the global Medical, Legal and Regulatory platform of Fresenius Kabi.
You will act as a link between Business, Medical, Legal, Regulatory, Quality, IT, suppliers, and regional stakeholders. You will translate business and compliance requirements into scalable product capabilities and ensure that the MLR platform supports harmonized, efficient, and compliant content review and approval processes worldwide.
Your tasks
- Ownership and communication of the global MLR product vision, roadmap, operating model, backlog, and strategic priorities.
- Functioning as the primary Business Owner and decision-maker for platform workflows, integrations, enhancements, and releases.
- Collaboration with Medical, Legal, Regulatory, Commercial, Quality, IT, Business Unit, and Country stakeholders to define global MLR processes and governance, translating business and compliance requirements into product requirements, User Stories, and acceptance criteria.
- Leading the entire product lifecycle – from discovery and design to launch, adoption, and continuous improvement – while harmonizing global processes with justified local and regulatory requirements.
- Leading the onboarding of Business Units and countries and ensuring rollout readiness, including planning, stakeholder alignment, training, communication, testing, and go-live preparation.
- Monitoring product performance, adoption, risks, and stakeholder feedback; prioritizing improvements and maintaining effective governance, documentation, compliance, and audit readiness.
- Managing platform providers and implementation partners to support the delivery and further development of the product.
- Collaboration with DAM (Digital Asset Management), CMS (Content Management System)/AEM (Adobe Experience Manager), CRM (Customer Relationship Management), and other Product Owners to build an integrated Commercial Content ecosystem, while providing easy support for PIM (Product Information Management) discovery, requirements, governance, and dependencies.
Your profile
- University degree in Business Administration, Life Sciences, Information Systems, or a comparable field.
- At least 8 to 12 years of experience in product management, MLR, digital platforms, Content Operations, or Business Analysis within Life Sciences or another regulated industry.
- Comprehensive understanding of MLR review and approval processes, Promotional Compliance, Claims and References, traceability, and Content Lifecycle Management; experience with MLR platforms such as Vodori, Veeva PromoMats, or similar solutions is very welcome.
- Experience with global transformations, Requirements Management, backlog prioritization, validation, UAT (User Acceptance Test), rollout, and adoption.
- Experience in managing Business Unit and Country stakeholders, suppliers, delivery partners, and cross-functional dependencies in global programs.
- Understanding of DAM, CMS, and Commercial Content Ecosystem integrations is an advantage.
- Strong skills in stakeholder management, influencing, communication, and decision-making, with the ability to translate complex business, compliance, and technical requirements into pragmatic product solutions.
- Business fluent English is required; additional languages are an advantage, as is the willingness to travel internationally.
We offer
See our Benefits page