Associate Director, Global Regulatory Sciences EU & International

Working with Us Challenging. 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. Some careers are built on execution. This one is built on ownership. There's a difference between being part of a regulatory strategy and being the person who defines it. If you've spent your career building towards that - the accountability, the influence, the genuine leadership - this is the role you've been preparing for. At Bristol Myers Squibb, we're looking for an Associate Director in Global Regulatory Sciences to own and drive EU and International regulatory strategy across the full product lifecycle. Not contribute to it. Not support it. Own it. What does ownership really look like here? It means when a programme needs a clear regulatory direction in Europe or internationally, you're the person who sets it. When health authorities have questions, you're the person leading the response. When cross-functional teams need a single point of accountability for EU and International regulatory topics - that's you. This is a role where the decisions you make, the strategies you define, and the relationships you build will have a direct line to patient access across multiple markets. That's not a talking point - it's the reality of what this work delivers. What you'll be doing and what you'll gain from it * Setting strategy, not receiving it. You'll own the EU and International regulatory strategy. You'll define registration scenarios, procedural pathways, timelines, and risk-mitigation approaches and you'll do it in close partnership with Global Regulatory Teams and Country Regulatory Managers. For you, this means stepping fully into strategic leadership and building a track record of regulatory outcomes that span geographies and product phases. * Leading at the table with Health Authorities. You won't just prepare for EMA interactions, you'll lead them. This is the kind of hands-on HA engagement that builds real authority, both within BMS and in the broader regulatory community. * Being the voice people turn to. You'll serve as the single point of accountability for European and International regulatory topics - the person who provides guidance, makes calls, and gives teams the clarity they need to move forward confidently. That kind of visibility accelerates careers. People will know your name, your judgement, and your impact. * Building and leading teams, not just working in them. You'll build and lead regulatory networks and share intelligence across functions and geographies. If you're at the stage where you want to shape the next generation of regulatory professionals and leave something behind beyond your own outputs - this is the platform to do it. * Owning labelling strategy end-to-end. You'll be accountable for target labelling strategies, and reference label implementation across the lifecycle. This is the kind of cross-cutting, high-visibility work that deepens your expertise and broadens your influence within the organisation. * With the potential to step into Global Regulatory Lead. Depending on programme needs and your experience, you may serve as Global Regulatory Lead with overall...