Associate Regulatory Director

At Bristol Myers Squibb our employees often ask Who are you working fora question that fuels collaboration accountability and urgency in our work. Our purpose-driven culture inspires us to discover develop and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work opportunities for growth and a supportive environment that values inclusion wellbeing flexibility and comprehensive benefits. This is work that transforms the lives of patients and the careers of those who do it.

• Take full responsibility for developing/implementing regulatory strategies on projects and achieving regulatory submission and approval for new products/ projects in therapeutic area within agreed timeline and deliverables taking into account to integrate future regulatory changes into the regulatory requirement.
• Ensure regulatory compliance with government policy and company required SOPs.

We hire for skills and capabilities not just credentials if this role excites you but doesnt perfectly match your resume we encourage you to apply anyway.

How We Work

Where you work matters because collaboration innovation and patient impact happen in many settings. Our roles are structured across four work models: site-essential site-by-design field-based and remote-by-design. The model assigned to this role is based on its core responsibilities. Learn more at People with Disabilities

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BMS will consider qualified applicants with arrest and conviction records pursuant to applicable laws in your area.

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