Associate Director, GRS - CMC, Cell Therapy

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 JobsAssociate Director, GRS - CMC, Cell TherapyWarsaw - PLApply NowFind out how well you match with this jobUpload your resumeJob descriptionLife at BMSWorking with UsChallenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.Why This Role?Regulatory science at its best isn't about paperwork — it's about getting transformative medicines to patients safely, efficiently, and without unnecessary delay. As an Associate Director within BMS's Global Regulatory Sciences – CMC team, you'll be the strategic bridge between the science of how a medicine is made and the global regulatory frameworks that govern how it reaches patients.This is a role for someone who wants to do more than review documents. You'll shape regulatory strategy for some of the most complex and exciting product types in modern medicine — small molecules, biologics, combination products, and cell therapies — and you'll do it at a company that is genuinely redefining what's possible in oncology, immunology, and beyond.If you're looking for a role where your expertise directly influences drug development timelines, global market access, and ultimately patient outcomes — this is it.What You'll Actually Be DoingOwning CMC Regulatory Strategy — End to EndYou'll be the primary regulatory CMC voice on cross-functional matrix teams, covering everything from early clinical trial applications through to new marketing authorizations, post-approval changes, and full lifecycle management. That means you won't just be executing someone else's strategy — you'll be developing it, owning it, and driving it forward independently.For candidates who've spent years waiting for a seat at the strategic table, this role puts you there from day one. Your input will directly shape how BMS navigates Health Authority expectations across global markets, with real consequences for program timelines and commercial outcomes.Being the Translator Between Science and RegulationOne of the most valuable things you'll do in this role is help technical teams understand what regulatory success looks like in practice. You'll interpret global regulations and guidance, identify where risks and opportunities lie, and help formulate mitigation strategies before problems become delays. You'll also anticipate regulatory paradigm shifts before they happen, giving BMS's development teams a competitive...