Senior Manager, Global Regulatory Sciences EU & International

Career Areas Career Stories Join Talent Community Candidate Login English English Italiano Español Français Português Norsk Deutsch 日本語 Bahasa melayu 中文 (简体) 中文 (繁體) 한국어 ภาษาไทย Nederlands Polski Yкраїнська Hrvatski Ελληνικά Magyar čeština Türkçe Pусский Haitian עברית Brazilian Português Dansk Suomi Svenska Français (Canada) Português (Portugal) Careers Home Life at BMS Career Areas Student Opportunities Events How We Recruit Career Stories Search this site Join Talent Community Candidate Login English English Italiano Español Français Português Norsk Deutsch 日本語 Bahasa melayu 中文 (简体) 中文 (繁體) 한국어 ภาษาไทย Nederlands Polski Yкраїнська Hrvatski Ελληνικά Magyar čeština Türkçe Pусский Haitian עברית Brazilian Português Dansk Suomi Svenska Français (Canada) Português (Portugal) Single PositionView All JobsSenior Manager, Global Regulatory Sciences EU & InternationalWarsaw - PL No longer accepting applications.Job IDR1601873Date posted04/26/2026DepartmentReg AffairsYour expertise could put life-changing medicines in the hands of patients across the globe.Think about what it means when a new therapy reaches a patient in Berlin or Warsaw. Behind that moment is a regulatory journey, high-stakes, and shaped by people like you.At Bristol Myers Squibb, we're looking for a Senior Manager in Global Regulatory Sciences to help navigate that journey across the EU and International regions. If you're someone who thrives on turning registration pathway into clear, strategic action and you want the work you do to genuinely matter, read on.This isn't a back-office compliance role. It's a seat at the table.You'll work at the heart of our global regulatory engine, partnering directly with Global Regulatory Leads and Country Regulatory Managers to shape end-to-end EU and International regulatory strategy.That means your thinking, your regulatory intelligence, and your ability to build alignment across teams will directly influence when and how patients access our medicines. That's a rare kind of impact.What you'll actually be doing and why it mattersShaping strategy, not just executing it. You'll define European submission plans, contribute to International regulatory strategies, and help set procedural timelines and risk assessments. You're not following someone else's roadmap, you're helping draw it. For you, this means growing your strategic muscles and building a body of work that spans multiple markets and therapeutic areas.Being the regulatory voice that others rely on. Cross-functional teams - from clinical to commercial - will look to you for regulatory guidance on EU and International topics. Whether it's input into clinical trial applications, variations, renewals, or paediatric and orphan designations, your expertise will help keep programmes moving and compliant. You'll build genuine credibility, both internally and externally.Engaging directly with Health Authorities. You'll contribute to and participate in interactions with the EMA and national authorities. This is hands-on experience that sharpens your regulatory acumen and expands your professional network in ways that stay with you throughout your career.Keeping your finger on the regulatory pulse. You'll monitor evolving guidelines, anticipate changes before they become problems, and escalate risks with solutions already in hand. Organisations value people who see around corners and this role gives you the platform to demonstrate exactly that.Supporting the team when it counts most. When time-critical situations arise - EU CTA queries, protocol amendments, urgent HA responses - you'll be part of the rapid response. You'll know how to stay calm, prioritise, and deliver. That kind of resilience is noticed and rewarded.The real gains, for youVisibility and influence - This is a recognised role within a global organisation. Your work won't be invisible. It feeds directly into portfolio decisions, launch readiness, and patient outcomes across multiple countries.Career acceleration -...