Radiopharmaceutical Production Operator II

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The Radiopharmaceuticals Production Operator will be an integral part of bringing RayzeBio’s innovative drug products to patients in need. As the Production Operator, you will play an active role in daily operations, striving to ensure each batch is right the first time and that the production area is kept in order at our manufacturing site in Indianapolis IN. You will be responsible for the production of RayzeBio drug products, strictly complying with good manufacturing practice and aseptic requirements. Additionally, you will be the front line in ensuring compliance with radiation safety requirements on the production floor.

As RayzeBio expands the production site and its portfolio of new products, the Production Operator will support validation work for future company initiatives, and support management with internal projects and new hire training. The Radiopharmaceuticals Production Operator will report directly to the Production Manager. Operator level will be evaluated with experience and qualifications.

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

Key Responsibilities:

• Execute production of RayzeBio drug products (including raw material preparation, line clearance and cleaning, equipment/instrument setup, etc.) while ensuring compliance with cGMP, aseptic practice, and management expectations.

• Support Production Management with training of new hires.

• Support and execute validation activities for clinical and commercial manufacturing.

• Support process improvements, both internally and cross-functionally, as opportunities present.

• Support department with inventory management, including cleaning supplies and personal protective equipment (PPE).

• Support day-to-day production operations, and upkeep of the production area.

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

Education and Experience:

• Previous experience working in a laboratory setting, particularly with pipetting and laminar flow hoods.

• 1 – 4 years’ experience operating in a GMP environment.

• Experience operating aseptically within ISO 7/Class C strongly preferred

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

• Strong attention to detail and precision in liquid handling

• Experience with radiochemistry and/or radiopharmaceuticals strongly preferred

Skills & Qualifications:

• Fluency in English.

• Strong knowledge of cGMP and aseptic practice.

• Knowledge of injectable and/or radiopharmaceutical drug product 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

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.

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