Supervisor, Isotope Production

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The Supervisor – Isotope Production, reporting to the Associate Director – Radiopharmaceuticals, will be an integral part of bringing RayzeBio’s innovative drug products to patients in need. As Supervisor – Isotope Production, you will be instrumental in implementing a novel isotope production program that will manufacture the clinical and commercial scale radioisotopes for RayzeBio’s drug products.  This individual will supervise a team of operators responsible for producing RayzeBio’s radioisotopes under Good Manufacturing Practices (GMP). Additionally, you will be the front line in ensuring compliance with radiation safety requirements on the production floor.  

*This is an onsite position at Rayzebio's Indianapolis, IN site

Job Responsibilities:

• Oversee day-to-day operations for RayzeBio’s radioisotope production (including scheduling, material preparation, line clearance, cleaning, equipment setup, and batch record execution) while ensuring compliance with GMP, NRC regulations, and management expectations.

• Supervise and develop a team of high-performing operators.

• Support Isotope Production Management with training of production staff.

• Support and execute validation activities associated with isotope production at the clinal and commercial scale.

• Work with cross-functional teams including Management, Radiochemistry and Engineering identifying opportunities to optimize production processes and enhance efficiency.

• Support Isotope Production Management in compiling KPIs and investigation of quality events (deviations, OOS, etc.).

• Support inventory management, including consumables, spare parts, cleaning supplies and personal protective equipment (PPE).

• Promote a culture of safety and compliance with EHS and Radiation Safety programs.

• Author and/or revise production technical documents (SOPs, forms, etc.) as needed.

Education and Experience:

• Proven experience in a supervisory role.

• 3 – 5 years’ experience operating in a GMP environment.

• Experience operating within hot cells and/or glove boxes strongly preferred.

• Associate’s or Bachelor’s Degree in a STEM field is preferred.

Skills and Qualification:

• Fluency in English.

• Strong knowledge of GMP practice.

• Knowledge of radiation safety principles.

• Knowledge of radiopharmaceutical manufacturing.

• Excellent professional ethics, integrity, and ability to maintain confidential information.

• Well organized and detail oriented.

• Strong interpersonal communication skills.

• Motivated, adaptable, and able to work under pressure while meeting the needs of the production schedule.

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If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol

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