Head Regulatory Information Management

Each day you'll enjoy a variety of challenges, such as:

• Delivering high-quality regulatory information management services for Grünenthal, including:

• RIM Product Championship (functional expertise, change management, training, and adoption of functionalities)
• RIM Process Management (harmonized, effective, and continuously improved business processes)
• RIM Data Management (effective, compliant, and aligned data management processes & standards)
• RIM Lifecycle Management (continuous development of RIMS platforms and adjacent technologies together with IT based on business needs)
• RIM Operations (high-quality regulatory operation services, including submission publishing)

Leading the evolution and prioritization of the GRA digital roadmap in close alignment with R&D Digital Transformation Office and IT

Driving the development of Regulatory Data Management & Governance capabilities aligned with R&D data strategy & governance

Enabling regulatory data analytics capabilities to maximize data value

Leading integration of RIMS with cross-functional systems and manages complex data landscapes

Defining and executing Grünenthal's regulatory data strategy to ensure compliance with evolving global regulations (e.g. IDMP, ESMP, eCTD 4.0)

Leading vendor selection, performance management, and external partnerships for GRA digital solutions and operations

Driving operational efficiency, resource optimization, and budget management for RIM services

Monitoring digital regulatory trends to ensure global readiness for upcoming requirements

Do you have experience in Presentation skills?, If you're passionate about changing lives for the better, this is the opportunity you've been waiting for. In Research & Development, we're continuously exploring innovative new treatment options to make a stronger, more positive impact on the lives of the patients we serve. You'll work with talented colleagues in a state-of-the-art Research & Development environment, developing innovative medicines that change the life of patients for the better and help us make progress towards our vision of a world free of pain. Join us today, and discover the difference you can make., * University degree in science, technology, or equivalent experience

• 10+ years of experience in regulatory information management within the pharmaceutical industry
• Strong knowledge of RIM processes across development and marketed products (EU & US required; LATAM a plus)
• In-depth understanding of relevant regulatory standards and regulations (e.g. IDMP, xEVMPD, eCTD, ESMP)
• 5+ years of hands-on experience with Veeva Vault RIMS and its business processes
• Experience with multiple RIM technologies and digital trends in Global Regulatory Affairs
• Global regulatory experience with a focus on EU and US
• Proven leadership and people development experience, driving high-performing teams
• Solid experience in budget, vendor, and contract management
• Strong project, people, change, and stakeholder management skills
• Excellent communication, negotiation, and presentation skills
• Strategic mindset with the ability to translate long-term vision into actionable goals
• Ability to work effectively in a matrix organization
• Excellent business English skills

Grünenthal is a global leader in pain management and related diseases. As a science-based, privately-owned pharmaceutical company, we have a long track record of bringing innovative treatments and state-of-the-art technologies to patients worldwide. Our purpose is to change lives for the better - and innovation is our passion. We are focussing all of our activities and efforts on working towards our vision of a world free of pain. Grünenthal is headquartered in Aachen, Germany, and has affiliates in 28 countries across Europe, Latin America and the US. Our products are available in more than 100 countries. In 2024, Grünenthal employed around 4,300 people and achieved sales of € 1.8 billion.