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Manager, Quality Control Microbiology, TerraPower Isotopes

TerraPower

Everett, WA

Full Time

Posted October 26, 2026

$205k - $205k

Nuclear Energy

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Application opens on company website

Listing evidence and provenance

Source: Greenhouse View original listing
Freshness: Open in the current public read path; this is not an employer guarantee.Last observed October 27, 2026
Classification: Modern power-system classification not yet published for this listing.Legacy source industry field: Nuclear Energy
Pay provenance: Employer-provided pay

Job Description

TerraPower Isotopes (TPI) is seeking an experienced Quality Control Manager to support production of Ac-225 at the Everett manufacturing facility.

Key Responsibilities

Provide operational leadership for the QC Microbiology team, including staffing, performance management, employee development, succession planning, and prioritization of laboratory activities.
Manage QC Microbiology laboratory operations supporting environmental monitoring, water systems, raw material testing, in-process testing, and product release testing.
Ensure QC laboratory operations are conducted in accordance with site safety requirements, biosafety standards, and radiological safety procedures.
Lead the development, qualification, validation, transfer, implementation, and lifecycle management of microbiological test methods and laboratory systems in compliance with cGMP and applicable regulatory requirements.
Accountable for end-to-end QC execution, data integrity, documentation, review, and reporting to support compliant batch disposition and Certificate of Analysis (CoA) issuance.
Own the development, implementation, maintenance, and continuous improvement of the site Contamination Control Strategy (CCS) in collaboration with Manufacturing, Engineering, Validation, Quality Assurance, and other cross-functional stakeholders.
Author, review, and approve SOPs, protocols, validation reports, specifications, and other GMP documentation related to microbiological testing and contamination control.
Lead risk assessments for contamination sources and recommend mitigation strategies throughout facility design, qualification, and routine operations.
Serve as the microbiology Subject Matter Expert (SME) during regulatory inspections, customer audits, and internal assessments.
Lead microbiology-related investigations, deviations, CAPAs, change controls, and quality risk management activities.
Oversee laboratory readiness, including equipment qualification, calibration, maintenance, media management, inventory control, and data integrity compliance.
Support installation, qualification, maintenance, and troubleshooting of instruments and laboratory systems used in radioisotope production.
Support management of laboratory chemical inventories, including procurement, storage, labeling, usage, and disposal in accordance with applicable regulations.
Drive continuous improvement initiatives related to laboratory automation, data management, reporting, Laboratory Information Management Systems (LIMS), and digital workflows.
Train and mentor QC personnel and operational staff on aseptic practices, microbiological controls, contamination prevention, and GMP expectations.
Build collaborative partnerships across Quality, Manufacturing, Engineering, Validation, Regulatory Affairs, and Radiation Safety functions.
Balance quality, operational, biosafety, and radiological safety requirements while maintaining a strong compliance-focused culture.

Requirements

Bachelor's degree in Microbiology, Biology, Biochemistry, or a related life sciences discipline; advanced degree preferred.
12+ years of relevant industry experience with a Bachelor's degree, 8+ years with a Master's degree, or 5+ years with a PhD; equivalent combinations of education and experience may be considered.
Minimum 3-5 years of progressive leadership experience managing technical or quality laboratory teams.
Extensive experience operating within FDA and cGMP-regulated environments, including 21 CFR Parts 210 and 211, ICH guidance, and applicable microbiological quality standards.
Experience supporting sterile manufacturing, radiopharmaceutical production, biologics manufacturing, or other highly regulated pharmaceutical operations preferred.
Demonstrated expertise in environmental monitoring, sterility assurance, contamination control, water systems monitoring, microbial identification, and microbiological method validation.
Strong working knowledge of EU GMP Annex 1 and Contamination Control Strategy (CCS) requirements.
Experience leading regulatory inspections, audits, investigations, CAPAs, and quality risk assessments.
Familiarity with radiological controls, radiation safety practices, and laboratory operations supporting radioisotope production is highly desirable.
Experience with LIMS, laboratory automation, electronic data management systems, and data integrity requirements.
Strong technical writing, documentation review, and communication skills.
Excellent analytical, troubleshooting, root-cause analysis, and problem-solving capabilities.
Demonstrated ability to build high-performing teams, develop talent, foster engagement, and create an inclusive culture.
Ability to adapt to changing priorities and work effectively in a dynamic manufacturing environment. Occasional off-shift or weekend support may be required.
The successful candidate will possess a high degree of trust and integrity, communicate openly, and display respect while fostering teamwork.

Benefits & Perks

Competitive Compensation
Salary, eligible to participate in discretionary short-term incentive payments
Comprehensive Medical and Wellness Benefits Medical Vision Dental Life and Disability Gender Affirmation Benefits
Parental Leave
401k Plan
Generous Paid Time Off (PTO) 21 days of annually accrued PTO
Generous Holiday Schedule 10 paid holidays
Relocation Assistance
Professional and Educational Support Opportunities
TerraPower Career and Benefits information: https://www.terrapower.com/careers/