Senior QC Microbiology Manager – Radiopharmaceuticals

Terrapower

Everett (WA)

On-site

USD 154,000 - 205,000

Full time

14 days+

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Benefits offered by this job

Relocation assistance
Professional and educational support
401k plan
21 days PTO

Job summary

TerraPower Isotopes is seeking an experienced Quality Control Manager to lead the QC Microbiology team at the Everett, WA facility supporting Ac-225 production. You will oversee environmental monitoring, method validation, and adherence to cGMP and radiological safety standards.

The role requires strong leadership, collaboration with Validation, Engineering, Regulatory Affairs, and Quality Assurance, and a focus on data integrity and continuous improvement of laboratory systems.

Qualifications

  • Bachelor's degree in Microbiology, Biology, Biochemistry, or related life sciences.
  • Advanced degree preferred for senior leadership.
  • 8+ years with a Master’s; 5+ years with a PhD; leadership experience required.

Responsibilities

  • Provide operational leadership for the QC Microbiology team and prioritize lab activities.
  • Manage QC Microbiology operations for environmental monitoring and product testing.
  • Ensure compliance with site safety, biosafety, and radiological safety procedures.
  • Lead development and validation of microbiological test methods and lab systems.

Skills

Leadership
Regulatory inspections
Microbiological testing
Environmental monitoring
Radiopharmaceutical production
Water systems monitoring
Quality risk management
Analytical method validation
Data integrity
Laboratory troubleshooting

Education

Bachelor's in Microbiology
Master's in relevant field
PhD (preferred)

Tools

LIMS
Laboratory automation
Electronic data management systems
Data integrity controls

Job description

TerraPower Isotopes is seeking an experienced Quality Control Manager to lead the QC Microbiology team at the Everett, WA facility supporting Ac-225 production. You will oversee environmental monitoring, method validation, and adherence to cGMP and radiological safety standards.

The role requires strong leadership, collaboration with Validation, Engineering, Regulatory Affairs, and Quality Assurance, and a focus on data integrity and continuous improvement of laboratory systems.

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