Radiopharmaceutical Production Operator I

Bristol-Myers Squibb Company; Guam; On-site; USD 43,000 - 52,000; Full time

Benefits offered by this job

Flexible Time Off

11 Paid Holidays

Volunteer Days

Job summary

RayzeBio, a wholly-owned subsidiary of Bristol Myers Squibb, seeks a Production Operator 1 to deliver radiopharmaceutical products at our Indianapolis facility. You will perform routine manufacturing tasks for a finished drug product program in a GMP environment, including formulation, filling, and equipment setup.

You will support validation activities, handle cleanings of isolators, and help maintain inventory and PPE while upholding safety and regulatory standards in a fast-paced lab setting.

Qualifications

• 1-2 years of experience operating in a GMP-regulated environment.
• High School diploma required; Associate’s degree preferred.
• Experience operating aseptically within ISO 7/Class C strongly preferred.
• Hands-on experience manufacturing pharmaceuticals or medical devices preferred.

Responsibilities

• Execute production of RayzeBio drug products, including raw material prep, line clearance, formulation, filling, and equipment setup, complying with cGMP and safety.
• Support and execute validation activities for clinical and commercial manufacturing.
• Perform cleaning and sanitization of CNC, ISO 8, ISO 7, and ISO 5 Isolators.
• Support process improvements and cross-functional collaboration.
• Assist inventory management and PPE supplies.
• Maintain production area and promote safety and compliance programs.

Skills

Attention to detail

Communication skills

Team collaboration

Adaptability

Ethics and integrity

GMP knowledge

Radiation safety knowledge

AI tools knowledge

Motivation under pressure

Confidentiality

Education

High School diploma

Associate’s degree preferred

Tools

Isolators operation

Job description

RayzeBio, a wholly-owned subsidiary of Bristol Myers Squibb, seeks a Production Operator 1 to deliver radiopharmaceutical products at our Indianapolis facility. You will perform routine manufacturing tasks for a finished drug product program in a GMP environment, including formulation, filling, and equipment setup.

You will support validation activities, handle cleanings of isolators, and help maintain inventory and PPE while upholding safety and regulatory standards in a fast-paced lab setting.