Teams at Bristol Myers Squibb

The Associate Director will drive European and International regulatory strategies across product lifecycles, ensuring registration success and compliance. Responsibilities include leading regulatory submissions, engaging with health authorities, and mentoring regulatory teams.

Lead Market Access learning strategy: define capability frameworks, prioritize role-based development, design onboarding curricula, set learning design standards, oversee content lifecycle, partner with field and cross-functional stakeholders, manage vendors, integrate learning into enterprise platforms, and measure effectiveness to drive continuous improvement.

Lead and execute root cause investigations for S12 CAR T operations, author reports, propose and verify CAPAs, support change control, audits, and cross-functional troubleshooting to ensure cGMP compliance and product/process risk mitigation.