Sr. Scientist, Radiopharmaceuticals

Life at BMS At RayzeBio, every day is an opportunity to ignite meaningful change. As a wholly-owned subsidiary of Bristol Myers Squibb, RayzeBio blends the nimble, pioneering spirit of an emergent biotech with the global expertise and resources of a leading innovator in oncology. Our mission is to develop transformative radiopharmaceutical therapies that offer new hope for patients living with cancer. Here, you’ll join a multidisciplinary team where your ideas are valued, your expertise is amplified, and collaboration is at the heart of everything we do. From day one, expect to make an immediate impact—on our science, on our teams, and most importantly, on patients. Learn more about RayzeBio:  https://careers.bms.com/rayzebio/ The Sr. Scientist, Radiopharmaceuticals will be responsible for advancing scientific and technical projects across various scientific, production, operations, quality and regulatory teams, to support development and commercialization  of radiopharmaceuticals. Responsibilities include driving preclinical development, Chemistry Manufacturing and Control (CMC), development and commercialization programs for drug products and radioisotopes.

Essential duties and responsibilities include the following.  Other duties may be assigned. · Design, plan and execute scientific experiments for preclinical development of radiopharmaceuticals. · Drive CMC process development and optimization for clinical drug products, including formulation lock and robust process definition, ensuring scalability and compliance with regulatory standards · Lead technology transfer of drug products and API from preclinical stage to clinical manufacturing. · Design, plan and execute scientific experiments for scale up and automation of drug products and API manufacturing processes. · Interpret complex experimental data, draw scientifically rigorous conclusions, and communicate findings in technical reports, regulatory documentation, and presentations for internal and external stakeholders · Author technical reports and source documents to support regulatory filing. · Author CMC sections for  IND/NDA for FDA submissions, and support regulatory filing in other jurisdictions, e.g. EMA, Health Canada, etc. · Collaborate cross-functionally with Regulatory, Quality, Supply Chain, Clinical, and R&D teams to ensure alignment with corporate goals · Manage and prioritize research projects, oversee third-party vendors, and mentor junior scientists and associates · Provide support for commercialization of radiopharmaceuticals · Uses AI tools to enhance individual productivity and quality of work · Up to 20% of travel required Education and Experience · Ph.D., M.S., or B.S. in Chemistry, Chemical Engineering, Pharmaceutical Sciences, or a related field, with requisite industry experience. · 5+ years of experience in drug development, manufacturing, CMC or related fields in a pharmaceutical industry, preferably radiopharmaceuticals. Skills and Qualifications · Strong understanding of GMP, FDA/EMA regulations, and ICH guidelines. · Strong problem-solving abilities and the ability to manage multiple projects in a fast-paced environment. · Excellent project management and cross-functional collaboration skills. · Excellent technical writing skills.

While performing the duties of this job, the employee is regularly required to sit, reach with hands and arms, and talk or hear. The employee must occasionally lift and/or move up to 15 pounds. Specific vision abilities required by this job include close vision and distance vision.  This is a position that requires working in a laboratory environment, protective clothing, gloves, and safety glasses are required while working in a laboratory environment with radioactive materials .

The noise level in the work environment is usually moderate. We hire for skills and capabilities, not just credentials – if this role