Senior Project Manager - TPI

Overview

TITLE:

Senior Project Manager

LOCATION:
Everett, WA or Bellevue, WA/Full-Time

The Terra Power Isotopes® (TPI™) has been established to pursue medical isotopes development--advancing nuclear science for significant human health benefits. We seek to support revolutionary radio therapies for treatments of various cancers through the supply of radioisotopes. TPI currently produces actinium-225 for the growing alpha therapy market and intends to expand.

The Terra Power Isotopes (TPI) business is an integral part of the Washington State based Terra Power 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. Terra Power’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. Terra Power 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.

In addition, as a federal contractor, Terra Power has instituted an Affirmative Action Plan (AAP) to proactively recruit, hire, and promote women, minorities, disabled persons and veterans.

• Lead the execution of a complex capital project spanning procurement, detailed design, install, commissioning, and validation of new manufacturing capabilities.
• Serve as the primary technical and execution integrator across internal engineering, quality, operations, and business stakeholders and external engineering, construction, and equipment partners.
• Drive technical decision-making and issue resolution to maintain project momentum, incorporating appropriate cross-functional input while protecting the critical path schedule.
• Work with the master scheduler to plan, manage, and maintain the integrated master schedule. Identifying risks, constraints, and opportunities and taking proactive action to preserve key milestones.
• Oversee vendor and contractor performance, including scope alignment, technical deliverables, schedule adherence, and change control.
• Ensure project execution aligns with applicable cGMP, quality, safety, and regulatory expectations, coordinating closely with Quality, Engineering, and Health Physics leadership.
• Monitor and communicate project status using clear, decision-focus reporting of schedule, cost, risks, and technical issues.
• Identify, assess, and escalate project risks and conflicts in a timely manner, recommending mitigation strategies and decision paths as needed.
• Maintain accurate project documentation, including schedules, risk registers, decision logs, and executive updates.
• Support engineering design reviews and readiness activities, coordinating required approvals while recognizing final engineering authority resides with the Directors of Engineering and Technology.

• B.S degree, with M.S., MBA or advanced degree preferred in Engineering, Chemistry, Pharmacy or related subject or relevant similar experience
• 5+ years of project management experience in a regulated environment (life sciences, biotech, pharma, nuclear, aerospace, medical device, or similar).
• Demonstrated success leading projects through design, procurement, installation and commissioning.
• Familiarity with cleanroom, containment (hot cell and glovebox), and facility retrofit projects strongly preferred
• Proficiency with Earned Value Management Systems (EVMS), risk management, and integrated scheduling tools.
• Strong working knowledge of project management software such as MS Project, Primavera, or equivalent.
• PMP certification (or equivalent) preferred.
• Familiarity with Good Manufacturing Practices (GMP), Quality by Design (QbD), and validation protocols.
• Strong…