Director, Global Labeling Strategy, Team Leader

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 . The Director, Global Labeling Strategy Team Lead - based in Warsaw - provides strategic leadership and oversight for a team of Global Labeling Strategists, driving labeling excellence especially across the Marketed Products Portfolio while shaping regulatory labeling strategy, policy, and innovation together with the Head of Global Labeling and relevant internal and external stakeholders.

Responsible for a team of Global Labeling Strategists primarily supporting the Marketed Product Portfolio As part of the Global Labeling Leadership team, contributes to build and execute the Global Labeling Strategy and Vision Acts as a strategic voice for Global Labeling Provides leadership and development for direct reports, establishing a framework facilitating knowledge sharing Builds a strong, future‑ready labeling organization through coaching, mentoring, succession planning, and capability development. Manages direct reports to ensure coverage for assigned products Ensures that Program Deliverables are met and labeling claims across programs / TA are consistent (including beyond the Marketed Product Portfolio) Leads key initiatives (Process Improvements, Development of new tools, technologies) to support efficient global label development and worldwide submissions, reviews and approvals Identifies opportunities to influence regulatory policy and climate with respect to labeling content Ensures effective planning of all cross-functional labeling activities Champions labeling modernization through digital labeling, structured content, data‑driven processes, and AI‑enabled solutions to improve speed, quality, and sustainability. Degree Requirements: Masters of Life Sciences or equivalent, with thorough understanding of scientific principles and at least 10 years of Labeling / Regulatory Experience; Bachelor of Lifesciences with at least 15 years of Labeling / Regulatory Experience; At least experience with one NME submission or Extension of Indication globally Advanced Academic Training (PharmD, PhD, MD) highly desirable Key Competency Requirements : Experience in people management, including but not limited to the development and management of (a) high performing team(s), with involvement of remote team members Knowledge of Global Labeling Guidances, Drug Development and Commercialization of prescription medicines Proven understanding of the dynamics and purpose of the Company Core Data Sheets (CCDS) and the implications of the CCDS Proven ability to understand regulatory implications of product strategy related to labeling development, assessment and management Demonstrated ability to develop strong and positive working relationships across diverse teams and within a global environment Proven Matrix leader with excellent problem-solving skills Ability to influence and lead a diverse group of Subject Matter Experts from a variety of disciplines and facilitate discussions and decision making Proven ability to develop and manage a highly competent and technically skilled team Experience in managing high to medium