Quality Control Microbiology Laboratory Supervisor

RayzeBio

Indianapolis, IN, US
Base: $107,904 - $130,754 annually; bonus/equity: ...
Fully remote
Cgmp regulated environment experience
Sterility and bioburden testing expertise
Environmental monitoring program management
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 oversee daily microbiology activities including sterility testing, environmental monitoring, and data trending while ensuring strict adherence to cGMP regulations and ALCOA+ principles.
  • Employees are eligible for comprehensive benefits including health coverage, a 401(k) plan, flexible time off, and potential incentive cash and stock opportunities.

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 annually; Bonus/Equity: Additional incentive cash and stock opportunities available; Benefits: Medical, dental, vision, 401(k), paid time off, and wellness programs

Skills & Requirements

Must-have

  • cGMP regulated environment experience
  • Sterility and bioburden testing expertise
  • Environmental monitoring program management
  • ALCOA+ data integrity principles
  • Aseptic technique and cleanroom gowning
  • Radiation safety program collaboration

Nice-to-have

  • Radiopharmaceutical operations experience
  • Process improvement and automation skills
  • Train-the-Trainer participation
  • Risk-based deviation investigation
  • Flexible schedule for off-shift support

Key Requirements

  • Bachelor's degree in Microbiology or related life science
  • Minimum 5 years of QC Microbiology experience in cGMP
  • Prior supervisory experience strongly preferred
  • Experience with sterile manufacturing highly desirable

Work Rights

Not specified

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