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Perspective Therapeutics

Clinical-stage radiopharmaceuticals using targeted alpha therapies

Manufacturing Engineer

Equipment MaintenanceConfirmed live in the last 24 hours
Full-timeChicago, IL, USANo salary listedIn-person

About the Job

Requirements

  • A bachelor's degree in an engineering or technical discipline, preferably Mechanical, Electrical, or Chemical Engineering, with five years of facilities-related experience; alternatively, five to eight years of relevant facilities maintenance experience in a cGMP facility, such as setup mechanic experience, may substitute for technical education.
  • Working experience using standard hand and power tools to perform maintenance-related work.
  • Working knowledge of Good Manufacturing Practices (GMP).
  • Basic electrical troubleshooting and repair experience in maintenance-related work.
  • Basic carpentry repair and painting experience in maintenance-related work.
  • Working knowledge of cGMP requirements and maintenance documentation practices.
  • Ability to use standard hand and power tools and perform basic electrical, carpentry, or mechanical tasks.
  • Valid driver's license, ability to lift up to 50 pounds, and willingness to work evenings, weekends, and holidays as needed.
  • Respirator fit test required.
  • Ability to maintain focus on a complex task for four to six hours at a time.
  • Ability to work independently with minimal direction and complete deliverables by provided deadlines.
  • Ability to work in a facility producing radioactive materials and participate in safety programs designed to minimize potential or actual exposure.
  • Ability to work indoors and outdoors around mechanical or moving parts and hazards including radioactive, corrosive, flammable, and toxic materials, dust, dirt, odors, and irritants.

Responsibilities

  • Own, support, and perform routine preventive maintenance on production, quality control, and safety equipment, including isolators, synthesis modules, glove testers, vaporized hydrogen peroxide systems, high-performance liquid chromatography systems, gamma counters, fume hoods, biosafety cabinets, and area monitors.
  • Troubleshoot equipment performance, maintenance, calibration, and commissioning or qualification problems.
  • Respond to production-related alarms; acknowledge, troubleshoot, and resolve alarm situations as needed or with supervisor assistance.
  • Manage maintenance work requests using a computerized maintenance management system, including accurate work-performance logs, material usage, and labor hours.
  • Author and execute change controls, commissioning and validation protocols, and technical documentation in alignment with Good Manufacturing Practices requirements.
  • Support investigations and root-cause analyses for equipment- or facility-related deviations or issues.
  • Participate effectively on project or major-repair teams and establish personal objectives aligned with group and organizational goals.
  • Provide support for fault-finding and root-cause analysis investigations as a developing technical resource.
  • Assist with cleanroom equipment relocation, renovations, and continuous-improvement activities requested by other departments.
  • Act as a point of contact for external service providers performing routine work, including preventive maintenance, calibration programs, and vendor-provided qualification, as well as on-demand breakdown and repair work.
  • Apply and promote safety rules and awareness, use appropriate protective equipment, and report and take initiative to correct safety and environmental hazards.
  • Manage lifecycle activities for Good Manufacturing Practice production, laboratory, and safety equipment at a newly constructed radiopharmaceutical manufacturing facility.
  • Support facility startup by assisting with commissioning, qualification, startup, and turnover of manufacturing and laboratory equipment.
  • Develop and implement preventive-maintenance and calibration strategies using the site's computerized maintenance management system.
  • Collaborate with equipment manufacturers and service providers and ensure equipment remains in a validated state throughout its operational lifecycle.
  • Work with Engineering, Manufacturing, Quality Assurance, Quality Control, Validation, Radiation Safety, and Environmental Health and Safety to support equipment reliability, regulatory compliance, and uninterrupted manufacturing operations.
  • Continue developing skills in automation, electrical and mechanical troubleshooting, and utilities operation.
  • Take ownership and accountability for assigned work and associated documentation.

About the Company

Perspective Therapeutics

Clinical-stage radiopharmaceuticals using targeted alpha therapies

Perspective Therapeutics develops targeted alpha-particle radiopharmaceuticals for cancer, using Lead-212 attached to tumor-targeting peptides and paired Lead-203 imaging for patient selection. It delivers potent alpha radiation to cancer cells to induce DNA damage while protecting healthy tissue, enabling theranostic treatment planning. The company differentiates itself with in-house development, a vertically integrated manufacturing and supply chain, and a radiopharmaceutical facility in New Jersey, plus a strategic partnership with Lantheus for funding and co-development. Its goal is to advance isotope-based cancer therapies from discovery to commercialization by building a reliable isotope supply network and expanding its therapeutic and diagnostic offerings.

Company size
51-200
Company stage
IPO
Headquarters
Seattle, WA
Founded
1998

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