Bristol Myers Squibb seeks a Manager, CMC Documentation & Specifications to join the Analytical Strategy & Operations team in Moreton, UK. You will author and coordinate CMC sections of regulatory submissions across small molecules, biologics, and ADCs, ensuring global regulatory standards and timelines are met.
You will lead small-molecule specification activities, coordinate regulator inquiries, and ensure data accuracy with rigorous attention to detail.
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CMC Documentation & Regulatory Writing Manager employer: Bristol Myers Squibb
At Bristol Myers Squibb, we offer a unique opportunity for Integrated Healthcare Managers to engage in meaningful work that truly transforms lives. Our supportive culture fosters professional growth and innovation, while our competitive benefits ensure a healthy work-life balance. Join us in the South UK, where you can thrive in a dynamic environment alongside passionate colleagues dedicated to making a real difference in the field of haematology-oncology.
