Job Description
Karo Healthcare, a dynamic and growing personal-care retail company, is all about making smart choices for everyday healthcare. With a wide-ranging portfolio across seven categories including medical products, we own and sell over 80 brands in about 90 countries. Our portfolio includes such brands as E45, Pevaryl, Lamisil, Nutravita, Decubal and many others. Our core belief in empowering people to make intelligent health decisions drives our growth strategy, blending organic expansion and M&A.
Join us at Karo Healthcare on our exciting journey. We’re currently looking for a Local Regulatory Affairs Manager Nordics for our office in Stockholm, Sweden.
What’s in it for you?
- Own and shape regulatory strategy for a high-impact Nordic portfolio in a fast-growing international FMCG environment
- Work hands-on with well-known brands while collaborating across global and local teams
- Accelerate your career in a dynamic company where regulatory is a true business partner
What you’ll be doing
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
University degree in Life Sciences or a related field
5+ years of Regulatory Affairs experience within Pharmaceuticals; exposure to other product categories is a plus
Strong knowledge of Nordic regulatory frameworks (experience with Norwegian regulations is an advantage)
Experience with artwork, labeling, and regulatory systems (e.g., Veeva RIM)
Proven ability to work cross-functionally in fast-paced, international environments and interact with regulatory authorities
Fluent in Swedish and English
Strong communication skills with a proactive, solutions-oriented and commercially minded approach
Structured, independent, and collaborative, with the ability to prioritize and drive work in a dynamic setting
Opportunity to create, grow, and encourage
Apart from a competitive salary pack, there are lots of growth opportunities to meet your personal ambitions
Flexible schedule, hybrid model with the primary work place in the office, and life-work balance
Responsibility for exciting and challenging projects that have a direct, visible impact on our customers and the industry
Very positive work environment in a dynamic, international, and motivated team
Start-up spirit while being a part of the large international organization with strong values
