Supervisor – Finished Drug Product Production
About The Position
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.
Requirements
- GMP compliance
- NRC regulations compliance
- Radiation safety best practices
- EHS compliance
Nice To Haves
- Experience in radio Finished Drug Product production
- Experience in clinical and commercial scale production
- Experience with operational KPIs
- Experience with quality event investigations (deviations, OOS, nonconformances)
- Experience with inventory management
- Experience authoring, reviewing, and revising production technical documentation (SOPs, forms, batch records)
Responsibilities
- Provide day‑to‑day operational oversight of radio Finished Drug Product production activities, including scheduling, material preparation, line clearance, equipment setup, and batch record execution, ensuring compliance with GMP, NRC regulations, and internal expectations.
- Serve as a functional lead for production operators by providing guidance, task coordination, and on‑the‑floor support to ensure safe, compliant, and efficient execution of manufacturing activities.
- Support onboarding and training efforts for production staff and promote adherence to GMP and radiation safety best practices during manufacturing activities.
- Support and execute validation activities associated with Finished Drug Product production at the clinal and commercial scale.
- Collaborate with cross‑functional partners including Quality, Safety, Engineering, Development, and Global Supply Chain to identify opportunities for process optimization, troubleshooting, and continuous improvement.
- Assist Finished Drug Product Production Management with the compilation of operational KPIs and support the investigation and resolution of quality events (e.g., deviations, OOS, and nonconformances).
- Support inventory management activities, including consumables, spare parts, cleaning supplies, and personal protective equipment (PPE).
- Promote and reinforce a strong culture of safety, quality, and compliance with EHS and Radiation Safety programs.
- Author, review, and revise production technical documentation (e.g., SOPs, forms, batch records) as needed to support manufacturing operations.
Benefits
- Medical, pharmacy, dental, and vision care
- BMS Well-Being Account
- BMS Living Life Better
- Employee Assistance Programs (EAP)
- 401(k) plan
- Short- and long-term disability
- Life insurance
- Accident insurance
- Supplemental health insurance
- Business travel protection
- Personal liability protection
- Identity theft benefit
- Legal support
- Survivor support
- Paid Time Off
- 11 paid national holidays
- Unlimited paid sick time
- 2 paid volunteer days per year
- Summer hours flexibility
- Leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs
- Annual Global Shutdown between Christmas and New Years Day
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
No Education Listed
