QC Microbiology Lab Supervisor – Radiopharma

Bristol-Myers Squibb; Indianapolis (IN); On-site; USD 108,000 - 131,000; Full time

Benefits offered by this job

Health insurance

Wellbeing programs

401(k) plan

Paid time off

Job summary

RayzeBio in Indianapolis is seeking a Quality Control Microbiology Laboratory Supervisor to oversee daily QC microbiology activities in a GMP radiopharmaceutical setting. You will supervise testing such as sterility, bioburden, endotoxin, and environmental monitoring, while ensuring ALCOA+ data integrity and regulatory compliance.

You will mentor staff, coordinate workloads, and partner with QA, Manufacturing, Facilities, and Radiation Safety to support product release and continuous

Qualifications

• Bachelor’s degree in Microbiology, Biology, or related life science discipline.
• Advanced degree (MS) preferred.
• Minimum 5+ years in QC Microbiology in a cGMP environment.
• Supervisory experience preferred.
• Experience with sterile manufacturing or radiopharmaceuticals desirable.

Responsibilities

• Supervise daily QC Microbiology activities including sterility, bioburden and endotoxin testing, media qualification and environmental monitoring.
• Review, approve and verify microbiological data and records for accuracy and ALCOA+ data integrity.
• Ensure calibration, qualification, and expiry of equipment, materials, and reagents.
• Support audits, regulatory inspections, and third‑party assessments; mentor analysts and technicians.
• Train and qualify personnel; coordinate workload to ensure on‑time, right‑first‑time testing.
• Collaborate with Manufacturing, QA, Facilities, and Radiation Safety to support production readiness.

Skills

Leadership

cGMP knowledge

GMP compliance

Data integrity

Regulatory awareness

Communication

Cleanroom work

Problem solving

Education

BS in Microbiology

MS preferred

Job description

RayzeBio in Indianapolis is seeking a Quality Control Microbiology Laboratory Supervisor to oversee daily QC microbiology activities in a GMP radiopharmaceutical setting. You will supervise testing such as sterility, bioburden, endotoxin, and environmental monitoring, while ensuring ALCOA+ data integrity and regulatory compliance.

You will mentor staff, coordinate workloads, and partner with QA, Manufacturing, Facilities, and Radiation Safety to support product release and continuous