Quality Assurance Specialist

TerraPower; Everett (WA); On-site; USD 117,000 - 152,000; Full time

Benefits offered by this job

Competitive compensation

Salary with discretionary incentive

Medical and wellness benefits

Parental leave

401k plan

Generous PTO (21 days)

Job summary

TerraPower Isotopes (TPI) seeks an experienced Quality Assurance Specialist to support Ac-225 production at the Everett, WA facility. The role focuses on GMP compliance, FDA Title 21 CFR 210/211, and ICH guidelines, with responsibilities spanning batch review, policy management, deviations, CAPA, supplier qualification, audits, and data integrity.

You will report to the Manager, Quality Assurance and collaborate with Operations, QC, Engineering, R&D, Procurement, and Commercial Services to

Qualifications

• Bachelor's degree in life sciences, engineering, or related field.
• 6+ years in regulated production; 3+ in QA.
• Experience with FDA cGMP Title 21 CFR 210/211 and ICH guidelines.
• Strong knowledge of quality systems and project management.
• Ability to balance compliance with production needs.

Responsibilities

• Review batch records, COAs, and documentation for accuracy.
• Author, revise, and manage approval of site policies and procedures.
• Review and approve quality documentation including deviations, change controls, CAPA, and complaints.
• Support supplier qualification, ensuring compliance with quality requirements.
• Provide QA support for ongoing production activities at Everett Laboratory.
• Support audits by preparing documentation, analyzing findings, and implementing corrective actions.
• Assist with quality system implementations and continuous improvement projects.
• Ensure data integrity across quality systems per ALCOA+ and 21 CFR Part 11.
• Balance quality with radiation safety in all activities.
• Provide QA training to colleagues and support inquiries.

Skills

Quality Assurance

Regulatory compliance

Documentation review

CAPA & deviations

Audit support

Cross-functional collaboration

Data integrity

Education

Bachelor's degree in life sciences/engineering or related field

Tools

Lean Six Sigma

Project Management

Job description

The TerraPower Isotopes® (TPI™) division has been established to pursue medical isotopes development--advancing nuclear science for significant human health benefits. We seek to support revolutionary radiotherapies for treatments of various cancers through the supply of radioisotopes. TerraPower currently has unique access to a supply of thorium for the long-term production of actinium-225 in the growing alpha therapy market and intends to expand into other nuclear related medical treatments.

The TerraPower Isotopes program is an integral part of the Washington State based TerraPower team, a company working to raise living standards globally. In 2006, the company originated with Bill Gates and a group of like-minded visionaries who evaluated the fundamental challenges to raising living standards around the world. TerraPower's mission is to be a world leader in new nuclear technologies, while developing innovators and future leaders in the nuclear field.

TPI is seeking to hire highly motivated and forward-thinking professionals who are interested in focusing on advanced radiopharmaceutical applications and influencing change within nuclear medicine. TerraPower is an Equal Opportunity Employer. We do not discriminate in hiring on the basis of sex, gender identity, sexual orientation, race, color, religious creed, national origin, physical or mental disability, protected veteran status, or any other characteristic protected by federal, state, or local law.

Quality Assurance Specialist - TPI

TerraPower Isotopes is seeking an experienced Quality Assurance Specialist to support Ac-225 production at the Everett, WA manufacturing facility.

The successful candidate will have experience in a quality assurance role with focus on ensuring compliance with Good Manufacturing Practices (GMP), regulatory guidelines (FDA Title 21 CFR 210/211 and ICH Guidelines), radiation safety, and company policies. The Quality Assurance Specialist will support the quality assurance activities including batch and material disposition, deviations, CAPA, change controls, authoring procedures and policies, supplier qualification and performance monitoring, audits, and system implementation. The position requires excellent judgement and discretion in balancing compliance and business resolutions. The Quality Specialist will report to the Manager, Quality Assurance and work closely with a multidisciplinary team including Operations, Quality Control, Engineering, R&D, Procurement, Project Management, and Commercial Services teams to achieve company objectives.

Responsibilities

• Review batch records, Certificates of Analysis, and documentation for accuracy and completion.
• Author, revise, and manage approval of site policies and procedures.
• Review and approval of quality documentation, including deviations, change controls and CAPA, and complaints.
• Support supplier qualification program, including verifying supplier compliance with applicable quality requirements, focusing on critical materials, services, and supplier performance.
• Provide Quality support for ongoing production activities at Everett Laboratory.
• Support internal and external audits by preparing documentation, analyzing findings, and implementing corrective actions.
• Support project workstreams and continuous improvement project driven by Quality.
• Support implementation of Quality Management Systems.
• Support development processes for validation/qualification of equipment, facility, and/or manufacturing processes.
• Ensure data integrity compliance across quality systems, including adherence to ALCOA+ principles and 21 CFR Part 11 requirements.
• Balance quality requirements with safety, such as radiation safety, in all quality activities.
• Provide comprehensive, Quality-related training to colleagues within TPI and act as a resource for quality related inquiries
• Perform other general duties associated with the position as required by supervision.

Key Qualifications and Skills

• Bachelor's degree in life sciences discipline, engineering, or a related field (or equivalent qualification through experience).
• 6+ years' industry experience in a regulated production environment (e.g., ISO 9001, cGMP pharmaceutical or radiopharmaceutical industries), including 3+ years of prior experience in a Quality Assurance role.
• Certification in a pharmaceutical Quality-related discipline, Lean Six Sigma or project management training/certification is a plus.
• Demonstrated experience working within Quality Systems.
• Strong working knowledge of quality principles, with proven success in managing complex projects and a wide range of responsibilities.
• Experience working within a quality program compliant to FDA/cGMP requirements Title 21 CFR 210/211 and ICH Guidance. Experience in a production radiopharmaceutical facility is preferred.
• Strong attention to detail, with the ability to interpret federal regulations, guidance and standards. Ability to incorporate relevant requirements into TPI documentation and provide guidance to personnel regarding compliance.
• Must demonstrate flexibility in adjusting to changing priorities and schedules in a dynamic environment. Occasional evening or weekend work might be required to support production operations or project deliverables.
• Strong interpersonal skills with demonstrated ability to lead cross-functional teams and drive accountability.
• Excellent written and verbal communication skills, including technical writing proficiency and executive-level reporting abilities.
• The successful candidate will possess a high degree of trust and integrity, communicate openly, and display respect while fostering teamwork.

Job Functions

Job Functions are physical actions and/or working conditions associated with the position. These functions may also constitute essential functions for the job which the employee must be able to fulfill, with or without accommodation. Information provided below is to help describe the job so that the applicant has a reasonable understanding of the job duties/expectations. An applicant's ability to perform and/or tolerate these actions and conditions will be discussed and workplace accommodations may be made on a case-by-case basis following an individualized assessment of the applicant and other considerations, including but not limited to any governing safety standards.

• Motor Abilities: Sitting for extended periods, bending/stooping, grasping/gripping, fine motor control (hands)
• Physical exertion and/or requirements: Minimal, with ability to safely lift up to 25 pounds.
• Repetitive work: Prolonged
• Special Senses: Visual and audio focused work
• Work Conditions: Stairs, typing/keyboard, standard and/or sitting working environment of >8 hours/day
• Travel required 0-10%

TerraPower Isotopes' technology is controlled for export by various agencies of the U.S. Government. TerraPower Isotopes must evaluate applicants who are foreign nationals (other than asylees, refugees, or lawful permanent residents) in accordance with U.S. Government export control requirements. To facilitate TerraPower's export control reviews, you will be asked as part of the application process to identify whether you are a U.S. Citizen or national, asylee, refugee, or lawful permanent resident of the United States. Government export authorization approval times vary. Based on the business needs for a particular position, TerraPower Isotopes may not consider a foreign national from a country if it is impracticable to obtain timely Government export approval.

Job details

Salary Range: $116,852 - $151,757

• We typically place offers in the lower to middle portion of the range to maintain internal equity and allow room for growth. Any salary offered within the posted salary band is based on market data and commensurate with the selected individual's qualifications experience. This range is specific to Washington State.

Benefits

• Competitive Compensation
• Salary, eligible to participate in discretionary short-term incentive payments
• Comprehensive Medical and Wellness Benefits
  • Medical
  • Vision
  • Dental
  • Life and Disability
  • Gender Affimation 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/