Head Regulatory Information Management (m/f/d)

Join our Research & Development team and work with talented colleagues in a state-of-the-art environment, developing innovative medicines that change the life of patients for the better.

Requirements

• 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

Benefits

• Competitive salary
• Benefits package
• Opportunity to work with a talented team in a state-of-the-art environment