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Quality Control Chemist - Isotope Production

Bristol Myers Squibb
Field - United States, United Statesfull_timeVerifiedPosted 10 Jun 2024

About the role

Working with Us
Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.

RayzeBio is seeking applicants for a Quality Control role in radioisotope production. The applicant will have experience in a cGMP environment with radioisopes, most ideally isotopes in the actinide series or other alpha emitters. The applicant will help build a quality control laboratory to analyze the radioisotopes, but will also be able to perform analysis on finished radiopharmaceuticals. Additionally, the applicant will be required to build a culture of radioisotope safety working with both internal and external stakeholders.

Job Responsibilities

• Perform analyses on radioisotopes (specifically radiometals) using ICP-MS, HPGe, radio TLC, and other modalities as deemed necessary.

• Assist in the technology transfer of analysis methods for radioisotope production.

• Work directly with production teams to schedule testing based on production needs.

• Perform analysis of finished radiopharmaceutical products as deemed necessary.

• Assist in writing and reviewing of laboratory Standard Operating Procedures (SOP’s) and related documents.

• Assist with the routine calibration and maintenance of all laboratory equipment and materials, and provide support for qualification and maintenance activities. On-board new instrumentation as required.

• Participate in troubleshooting and investigations of analytical issues, identify root causes, and implement corrective actions as required.

• Develop and maintain appropriate documentation, particularly data analysis.

• Ensure compliance with GMP regulations, safety guidelines, and quality standards.

• Work with RSO to ensure laboratory compliance with radiation safety programs.

• Provide technical support to other teams or business units as required.

• Provide technical expertise and support for offsite vendors and RayzeBio MS&T and RA/QA teams in the installation and qualification of all laboratory equipment in a GMP environment.

• Mentor junior chemists, as necessary.

• Position is a salaried, first shift position. Work outside first shift is expected on an as-needed basis.

• Up to 15% of travel may be required.

Qualifications

• BS in chemistry or related field with 5+ years of experience in pharmaceutical or radioisotope field OR MS in chemistry or related field with 3-7 years of experience in pharmaceutical or radioisotope field.

• Experience handling radioactive materials essential.

• Experience testing in a quality control chemistry lab is required.

MS in chemistry or related field with 3- 7 years of experience in the pharmaceutical or radioisotope field.

Skills

• It is essential the candidate set a radiation safety culture in the lab through communication with both internal and external stakeholders.

• Experience with radiopharmaceuticals and/or radioactive isotopes is required; experience with elements in the actinide series is strongly preferred. Experience with other alpha emitters will be considered.

• Highly motivated and organized professional with the ability to work independently or in a team environment.

• Multi-disciplined scientist with GMP experience.

• Experience with root cause techniques such as 6 M’s, 5 Why’s, fishbone, or similar preferred.

• Ability to multi-task and prioritize work based on multiple work-flows.

• Good organizational skills are required.

• Work with multiple computer systems, including Microsoft Office, and chromatography systems.

• Excellent professional ethics, integrity, and ability to maintain confidential information.

The starting pay rate takes into account characteristics of the job, such as required skills and where the job is performed.

Final, individual compensation will be decided based on demonstrated experience.

Benefit offerings are sub

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Company

Bristol Myers Squibb

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