Radiopharma Production Operator I

Bristol-Myers Squibb; Indianapolis (IN); On-site; USD 89,027,000 - 107,854,000; Full time

Benefits offered by this job

Medical, dental, vision coverage

401(k) plan with company match

Life and disability insurance

Paid time off and holidays

Job summary

RayzeBio, a wholly-owned subsidiary of Bristol Myers Squibb, seeks an Operator I for its Indianapolis facility to execute production of radiopharmaceuticals under cGMP and aseptic conditions. This role supports validation activities for clinical and commercial manufacturing and contributes to process improvements with cross-functional teams.

Ideal candidates have lab experience, 1–4 years in GMP environments, and background in radiochemistry or related fields.

Qualifications

• GMP experience in a lab/plant environment is required.
• Experience with aseptic operations and cleanroom practices is preferred.
• Experience with radiochemistry/radiopharmaceuticals is a plus.
• Hands-on lab experience and ability to work in controlled environments.

Responsibilities

• Execute production of radiopharmaceutical drug products with proper GMP, aseptic technique, and equipment setup.
• Support validation activities for clinical and commercial manufacturing.
• Assist with inventory management and PPE supplies.
• Maintain a safe, compliant production area and participate in EHS programs.
• Other duties as assigned.

Skills

GMP knowledge

Radiation safety

Ethics and confidentiality

Organized and detail-oriented

Interpersonal communication

Adaptable and works under pressure

AI tools usage

Education

STEM degree preferred

Tools

Pipettes

Laminar flow hood

Hot cells

Gloveboxes

Job description

RayzeBio, a wholly-owned subsidiary of Bristol Myers Squibb, seeks an Operator I for its Indianapolis facility to execute production of radiopharmaceuticals under cGMP and aseptic conditions. This role supports validation activities for clinical and commercial manufacturing and contributes to process improvements with cross-functional teams.

Ideal candidates have lab experience, 1–4 years in GMP environments, and background in radiochemistry or related fields.