Quality Control Microbiology Laboratory Supervisor

RayzeBio

Indianapolis, IN, US
Base: $107,904 - $130,754; bonus/equity: + incenti...
Fully remote
Bachelor's degree in microbiology or related life science
Minimum 5 years experience in cgmp regulated environment
Prior supervisory experience in qc microbiology laboratory
This role offers the opportunity to join a multidisciplinary team at RayzeBio, a subsidiary of Bristol Myers Squibb, to develop transformative radiopharmaceutical therapies for cancer patients

Job Summary

  • This role offers the opportunity to join a multidisciplinary team at RayzeBio, a subsidiary of Bristol Myers Squibb, to develop transformative radiopharmaceutical therapies for cancer patients.
  • The supervisor will provide oversight for daily microbiology activities, ensuring data trending, troubleshooting, and compliance with regulatory and QA system requirements for radioisotopes.
  • Compensation ranges from $107,904 to $130,754 annually, with additional incentive cash, stock opportunities, and comprehensive benefits including health coverage and paid time off.

Matching Summary

This role offers the opportunity to join a multidisciplinary team at RayzeBio, a subsidiary of Bristol Myers Squibb, to develop transformative radiopharmaceutical therapies for cancer patients.

Salary

Base: $107,904 - $130,754; Bonus/Equity: Additional incentive cash and stock opportunities available; Benefits: Medical, dental, vision, 401(k), PTO, and wellness programs

Skills & Requirements

Must-have

  • Bachelor's degree in Microbiology or related life science
  • Minimum 5 years experience in cGMP regulated environment
  • Prior supervisory experience in QC Microbiology laboratory
  • Strong knowledge of USP <61>, <62>, <71>, <85> and EU GMP Annex 1
  • Ability to work in classified cleanroom environments with gowning
  • Experience with sterility testing, bioburden testing, and endotoxin testing

Nice-to-have

  • Advanced degree (MS) in Microbiology or Biology
  • Experience supporting sterile manufacturing operations
  • Experience supporting radiopharmaceutical operations
  • Knowledge of radiation safety program collaboration
  • Ability to use AI tools to enhance productivity
  • Flexible schedule including weekend or off-shift support

Key Requirements

  • BS in Microbiology required; MS preferred
  • 5+ years QC Microbiology experience in cGMP environment
  • Prior supervisory experience strongly preferred
  • US work authorization required (implied by location)

Work Rights

Not specified

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