Radiopharma Production Operator (Aseptic)

Bristol-Myers Squibb Co; Indianapolis (IN); On-site; USD 43,000 - 52,000; Full time

Benefits offered by this job

Comprehensive benefit plans

Flexible Time Off (FTO)

11 paid company holidays

Job summary

RayzeBio, a wholly-owned subsidiary of Bristol Myers Squibb, seeks an Operator 1, Production in Indianapolis, IN to perform routine execution of a finished drug product program for radiopharmaceuticals. You will work under the Production Supervisor on clinical and commercial-scale manufacturing with emphasis on quality and safety.

The role requires 1–2 years in a GMP setting, HS diploma (associate degree preferred), and willingness to work in a lab with radioactive materials.

Qualifications

• Hands-on experience in GMP-regulated environments.
• Knowledge of radiation safety principles is preferred.
• Experience manufacturing pharmaceuticals or medical devices is a plus.
• Aptitude for working in a laboratory with protective equipment and radioactive materials.

Responsibilities

• Execute production of RayzeBio drug products including preparation, line clearance, formulation, filling, and equipment setup while following cGMP and aseptic practices.
• Support and execute validation activities for clinical and commercial manufacturing.
• Perform cleaning and sanitization of ISO 7/Class C isolators.
• Support process improvements across functions as opportunities arise.
• Assist inventory management for cleaning supplies and PPE.
• Support daily production operations and upkeep of the production area.
• Promote safety and compliance with EHS and Radiation Safety programs.

Skills

GMP practices

Radiation safety

AI tools

Interpersonal communication

Detail oriented

Ethics and confidentiality

Education

High School diploma

Associate’s degree preferred

Job description

RayzeBio, a wholly-owned subsidiary of Bristol Myers Squibb, seeks an Operator 1, Production in Indianapolis, IN to perform routine execution of a finished drug product program for radiopharmaceuticals. You will work under the Production Supervisor on clinical and commercial-scale manufacturing with emphasis on quality and safety.

The role requires 1–2 years in a GMP setting, HS diploma (associate degree preferred), and willingness to work in a lab with radioactive materials.