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Quality Control Microbiology Laboratory Supervisor

Bristol Myers Squibb
September 15, 2026
Full-time
On-site
Indianapolis, IN
Operations
Role: Lead oversight of microbiology QC activities supporting GMP manufacturing of radiopharmaceuticals at RayzeBio's Indianapolis site. Objectives include ensuring regulatory compliance, data integrity, and high-quality product release. Responsibilities encompass supervising microbiology testing (sterility, bioburden, endotoxin, environmental monitoring), maintaining aseptic techniques, reviewing data, managing equipment qualification, and supporting audits. The supervisor also mentors staff, collaborates with manufacturing, QA, radiation safety, and supports process improvements. Qualifications: Bachelor's in Microbiology, Biology, or related; 5+ years in cGMP microbiology labs; prior supervisory experience preferred. Experience with sterile manufacturing and radiopharmaceuticals highly desirable. Skills include leadership, knowledge of cGMP, USP, EU GMP, data integrity, and microbiological methods. High-value biopharma specifics: GMP, radiopharmaceuticals, sterile QC, microbiology, radiation safety compliance, and support for radiopharma production. Location: Indianapolis, IN; work involves working with ionizing radiation and hazardous chemicals. The role may require occasional off-shift or weekend work.