Cyclotron Engineer: PET Isotope Ops & On-Call

PharmaLogic; Gray (TN); On-site; USD 75,000 - 90,000; Full time

Benefits offered by this job

Bonus 10%

On-site work

Job summary

PharmaLogic is seeking a Cyclotron Engineer to support PET site operations through routine maintenance of cyclotron equipment and related systems. The role emphasizes GMP compliance, safety, and meticulous documentation to ensure quality and reliability of radiopharmaceutical production.

Responsibilities include maintenance, calibration, on-call support, and collaboration with Quality and Facility teams to meet production schedules and regulatory requirements.

Qualifications

• Completion of manufacturer\'s applications training course for the cyclotron and chemistry modules.
• Experience in PET manufacturing, pharmaceutical manufacturing (FDA and GMP regulated), nuclear pharmacy, chemistry training or comparable laboratory background preferred.
• Bachelor\'s degree in science preferred or technical degree, electronics military training or equivalent experience.
• Knowledge of cGMP and NRC regulations preferred.
• Strong interpersonal skills with effective communication across diverse populations.
• Computer proficiency including Word, Excel, and Outlook.

Responsibilities

• Maintains favorable working relationships to promote productivity.
• Works with radioactive materials and follows ALARA procedures.
• Ensures completion of required equipment maintenance and calibration.
• Documents out of specification (OOS) or deviations for GMP compliance.
• Coordinates with Facility Manager for preventive maintenance and downtime.
• Operates and maintains the PET cyclotron; supports isotope production.

Skills

Cyclotron maintenance

GMP compliance

Electrical troubleshooting

Diagnostic equipment knowledge

Education

Bachelor's degree in science or technical field

Tools

Microsoft Office

Job description

PharmaLogic is seeking a Cyclotron Engineer to support PET site operations through routine maintenance of cyclotron equipment and related systems. The role emphasizes GMP compliance, safety, and meticulous documentation to ensure quality and reliability of radiopharmaceutical production.

Responsibilities include maintenance, calibration, on-call support, and collaboration with Quality and Facility teams to meet production schedules and regulatory requirements.