Nordic Regulatory Affairs Manager

Join Karo Healthcare as a Nordic Regulatory Affairs Manager to shape regulatory strategy for a high-impact Nordic portfolio in a fast-growing international FMCG environment. Collaborate with global and local teams to accelerate your career in a dynamic company where regulatory is a true business partner.

Requirements

• Drive end-to-end regulatory activities across product classifications, ensuring timely submissions and approvals
• Manage lifecycle activities for pharmaceutical products
• Lead communication with regulatory authorities and relevant bodies
• Review artworks and commercial materials to ensure compliance
• Provide strategic regulatory input to enable product launches and market access
• Support local implementation of global NPD, EPD, and GeoX projects
• Perform pragmatic risk assessments balancing compliance with business needs
• Ensure accurate and compliant data in Veeva RIM and artwork systems
• Secure compliant product information, translations, and labeling
• Maintain national databases and product information platforms
• Collaborate closely with Global RA and cross-functional teams across Commercial, Supply Chain, and Scientific Affairs
• Contribute to regulatory input in business decisions and growth initiatives
• Participate in commercial activities such as customer trainings, conferences, and events
• Bring customer and market insights into regulatory and business decisions

Benefits

• Competitive salary pack
• Flexible schedule
• Hybrid model with the primary work place in the office
• Life-work balance
• Responsibility for exciting and challenging projects
• Very positive work environment
• Growth opportunities
• Start-up spirit with a large international organization