Global Regulatory Affairs Manager, Pharma Strategy
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- Key details
- 1 location, Finance, Legal & Compliance, Hybrid, Full time
- Current openings
- 13 active jobs
- Original language
- English
- Source and freshness
- Collected from public career pages and reviewed through JobGrid.eu source availability checks. Last verified: May 13, 2026.
- Apply path
- JobGrid.eu sends candidates to the original application page and adds non-personal referral parameters.
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 Global Regulatory Affairs Manager, Pharma Strategy for our office in Stockholm.
What’s in it for you?
- Own and drive global regulatory strategy in a fast-growing, international environment
- Work cross-functionally with senior stakeholders and make real business impact
- Gain exposure to product launches and lifecycle management across markets
- Be part of a hands-on, entrepreneurial culture with strong growth opportunities
What you’ll be doing
- Lead global regulatory strategy and act as RA project lead for key initiatives (MAAs, M&A, NPD, EPD)
- Drive regulatory planning, execution, and submissions across multiple markets
- Prepare and review core regulatory documentation (Modules 2, 4, 5) and authority responses
- Manage submissions including variations, PSURs, and renewals
- Collaborate cross-functionally with Scientific Affairs, Operations, and Commercial teams to ensure alignment and execution
- Act as the regulatory voice in strategic discussions, influencing business decisions
- Build and maintain strong relationships with regulatory authorities
- Develop and continuously improve SOPs and regulatory processes