Regulatory CMC Director

3 weeks ago


Uxbridge, United Kingdom Bristol Myers Squibb Full time
Job Summary

Bristol Myers Squibb is seeking a highly skilled Regulatory CMC Director to join our team. As a key member of our Global Regulatory Sciences organization, you will be responsible for developing and implementing global regulatory strategies for biologics and cell therapy products. This is a unique opportunity to work with a talented team of professionals who are passionate about transforming patients' lives through science.

Key Responsibilities
  • Develop and implement global regulatory strategies for biologics and cell therapy products
  • Collaborate with cross-functional teams to ensure regulatory compliance and effective product development
  • Provide regulatory expertise and guidance to internal stakeholders on CMC-related matters
  • Prepare and submit regulatory filings and responses to health authorities
  • Stay up-to-date with global regulatory requirements and trends in the biopharmaceutical industry
Requirements
  • Minimum 10+ years of experience in regulatory affairs, with a focus on biologics and cell therapy products
  • Proven track record of developing and implementing successful regulatory strategies
  • Strong knowledge of global regulatory requirements and trends in the biopharmaceutical industry
  • Excellent communication and collaboration skills
  • Ability to work in a fast-paced environment and prioritize multiple tasks and projects
What We Offer

Bristol Myers Squibb is committed to creating a diverse and inclusive work environment that fosters innovation and collaboration. We offer a competitive salary and benefits package, as well as opportunities for professional growth and development. If you are a motivated and talented individual who is passionate about regulatory affairs, we encourage you to apply for this exciting opportunity.



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