Rad iochemistry Associate Scientist II – GMP & Radiolabeling

Bristol Myers Squibb; Indianapolis (IN); On-site; USD 47,000 - 57,000; Full time

Job summary

RayzeBio, a wholly-owned subsidiary of Bristol Myers Squibb, is seeking an Associate Scientist II to perform routine operations in the development laboratory at our Indianapolis facility. The role supports radiochemical and analytical methods for drug product, QC, and isotope supply as we advance radiopharmaceuticals from R&D to GMP manufacturing.

You will handle routine equipment checks, GMP radiolabeling, QC support, inventory, onboarding of new technologies, and participate in expansion

Qualifications

• BS with 0-3 years of radiochemistry or related scientific experience.
• Experience with GMP and GDP is desirable.
• Experience with radioactive materials is desired.

Responsibilities

• Execute routine equipment checks and maintenance following GDP/GMP guidelines.
• Independently perform routine GMP radiolabeling and clinical site sample preparation.
• Support general laboratory organization and cleanliness.
• Support scientific team performing development work related to RayzeBio’s drug product pipeline and programs.
• Manage third party vendors in support of analytical and laboratory equipment.
• Support activities related to hot cells, gloveboxes, and production cleanrooms.
• Ensure compliance with NRC, EH&S and US/EU GMP regulatory guidelines as required.
• Less than 5% of travel required

Skills

Lab safety

GMP/GDP experience

Analytical methods

Radioactive materials

Independent work

Team collaboration

AI tools usage

Education

BS in Radiochemistry

Experience with radioactive materials

GMP/GDP knowledge

Job description

RayzeBio, a wholly-owned subsidiary of Bristol Myers Squibb, is seeking an Associate Scientist II to perform routine operations in the development laboratory at our Indianapolis facility. The role supports radiochemical and analytical methods for drug product, QC, and isotope supply as we advance radiopharmaceuticals from R&D to GMP manufacturing.

You will handle routine equipment checks, GMP radiolabeling, QC support, inventory, onboarding of new technologies, and participate in expansion