Scientific affairs Specialist - Central Europe job opportunity at Karo Healthcare.

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Date2026-02-11T11:04:58.262Z bot
Karo Healthcare Scientific affairs Specialist - Central Europe
Experience: 2-years
Pattern: Full-time
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loacation Warsaw, Poland
loacation Warsaw....Poland
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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 Scientific Affairs Specialist – Central Europe for our office in Warsaw. What’s in it for you? Make real impact across 10 markets in Central Europe, working at the intersection of science, compliance, and commercial execution. Gain hands-on international exposure in a fast-growing, M&A-driven healthcare company with strong FMCG dynamics. Accelerate your development in regulatory affairs, pharmacovigilance, and product compliance within a high-performing, collaborative team. What you’ll be doing Act as the local Scientific Affairs expert across Central Europe (Germany, Switzerland, Austria, Poland, Czech Republic, Slovakia, Slovenia, Bulgaria, Hungary, Romania) Serve as the key link between Global Scientific Affairs and local commercial teams, ensuring product quality, patient safety, and regulatory compliance Be the first point of contact for pharmacies, healthcare professionals, authorities, and consumers for complex product inquiries and complaints Manage compliant product launches, including submissions to local Health Authorities (eAF, cover letters, PoA, translations, labeling, artwork process) Lead local drug shortage reporting in collaboration with Global QA Oversee local pharmacovigilance activities, acting as Local PV Contact and authority-facing representative Monitor and manage safety case reporting, adverse events, and relevant literature in line with GVP requirements Review and approve marketing materials and claims, ensuring promotional compliance Support commercial teams as a compliance sparring partner in a fast-paced environment Contribute to local SOP updates and Global Quality Management System implementation Deliver PV and compliance training to affiliates, partners, and distributors Requirements Master’s degree in Pharmacy 1–2 years’ experience in Regulatory Affairs, Quality, or Scientific Affairs within healthcare, pharma, medical devices, or FMCG-related industries Experience in local pharmacovigilance activities is a strong advantage Solid understanding of compliance, product lifecycle management, and health authority interactions Fluent in English and Polish; German is a plus Structured, proactive, and solution-oriented mindset Comfortable working cross-functionally in an international, fast-moving organization Strong communication skills and high level of diligence and accountability

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