Radiochemistry QC Associate Scientist I

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

Benefits offered by this job

Flexible Time Off

Comprehensive benefits package

Job summary

RayzeBio in Indianapolis seeks an Associate Scientist I for Quality Control to execute testing supporting isotope production and material release. You will inspect raw materials, in-process controls, and finished products, ensuring specifications and regulatory standards are met.

This role emphasizes timely data generation, recordkeeping, and adherence to GMP practices. The ideal candidate has a chemistry background with 0–3 years in analytical or radiochemistry, strong documentation skills, and

Qualifications

• Bachelor's degree in Chemistry or related scientific discipline with 0–3 years of experience.
• Knowledge of GMP/ISO and documentation practices is preferred.
• Experience in analytical chemistry or radiochemistry.
• Strong attention to detail and documentation accuracy.

Responsibilities

• Perform routine analyses according to validated methods to support isotope production.
• Record data and analyze results to ensure timely final product testing and release.
• Assist in development and improvement of laboratory SOPs and related documents.
• Ensure proper calibration and maintenance of lab equipment.
• Maintain compliant documentation and data analysis records.
• Support instrument qualification, calibration, and maintenance activities.
• Collaborate with Radiation Safety Officer to ensure radiation safety compliance.
• Provide technical support to other teams as needed.

Skills

Quality control testing

GLP experience

Analytical chemistry

Radiochemistry

Recordkeeping

Data analysis

SOP development

AI tools usage

Education

Bachelor's degree in Chemistry or related field

Job description

RayzeBio in Indianapolis seeks an Associate Scientist I for Quality Control to execute testing supporting isotope production and material release. You will inspect raw materials, in-process controls, and finished products, ensuring specifications and regulatory standards are met.

This role emphasizes timely data generation, recordkeeping, and adherence to GMP practices. The ideal candidate has a chemistry background with 0–3 years in analytical or radiochemistry, strong documentation skills, and