Advanced Radiopharmaceutical Production Operator II

Telix Pharmaceuticals (AMER)

Pennsylvania

On-site

USD 65,000 - 90,000

Full time

12 days ago

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Benefits offered by this job

Competitive salary
Annual bonuses
Equity incentives
Generous vacation
Wellness days
Learning & development

Job summary

Telix Pharmaceuticals is seeking a Radiopharmaceutical Production Operator I to support routine synthesis, QC, and production of PET radiopharmaceuticals in a cGMP facility in Wilkes-Barre, PA.

You will perform aseptic synthesis and document results, ensuring compliance with GMP and radiation safety standards. The role requires an Associates degree or certifications and 2+ years in a lab, with readiness for shift coverage and on-site work.

Qualifications

  • Associates degree or certifications in chemistry, radiochemistry or a related field.
  • 2+ years of experience in a laboratory setting, preferably radiopharmaceuticals.
  • Knowledge of radiochemical synthesis, purification, and safe handling of radioactive materials.
  • Experience with precision measurement equipment.
  • Ability to read and interpret engineering drawings, specifications, and manufacturing work instructions.
  • Strong problem-solving skills and attention to detail.
  • Ability to work in a team environment and communicate effectively with diverse groups.
  • Familiarity with GMP and radiation safety practices.

Responsibilities

  • Executes routine synthesis, dispensing and QC sampling steps independently and in sequence, while maintaining aseptic technique and contamination control discipline.
  • Identifies processes drifting from the defined window and escalates before proceeding.
  • Assist in process qualification and process improvement initiatives working with cross functions teams.
  • Supports commissioning and equipment qualification activities.
  • Executes quality control testing using analytical instrumentation (TLC, HPLC, GC); analyzes and interprets results against established specifications and documents outcomes in compliance with GxP requirements.
  • Participates in inspections, maintenance, and troubleshooting to support manufacturing and testing processes and equipment.
  • Implements approved SOP changes to production and quality control processes, helping drive continuous improvement.
  • Performs daily, weekly, monthly, and quarterly PM checks of cyclotrons, chemistry modules, and QC equipment per SOPs.
  • Oversees routine logistics functions, including preparing product for shipment, coordinating courier schedules, and documenting as necessary.
  • Identifies opportunities for efficiency in the production process.
  • Maintains a clean, clutter-free facility and a well-organized production area and workflow.
  • Train and mentor Radiopharmaceutical Production Operator I
  • Provides exemplary customer support.
  • Other tasks as assigned by supervisor.

Skills

Radiochemical synthesis
Purification
Radioactive materials safety
GxP knowledge

Education

Associates degree or certifications in Chemistry, Radiochemistry, Biochemistry, or a related field

Tools

TLC
HPLC
GC

Job description

Telix Pharmaceuticals is seeking a Radiopharmaceutical Production Operator I to support routine synthesis, QC, and production of PET radiopharmaceuticals in a cGMP facility in Wilkes-Barre, PA.

You will perform aseptic synthesis and document results, ensuring compliance with GMP and radiation safety standards. The role requires an Associates degree or certifications and 2+ years in a lab, with readiness for shift coverage and on-site work.

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