Actinium-225 & Medical Isotopes Production Specialist

Terrapower

Everett (WA)

Presencial

USD 94.000 - 122.000

Jornada completa

Hace 8 días

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Ventajas ofrecidas por este puesto de trabajo

Competitive compensation
Discretionary incentive payments
Medical and wellness benefits
Paid time off
Relocation assistance
Professional and educational support

Descripción de la vacante

TerraPower Isotopes is seeking a Radioisotopes Production Specialist to produce actinium-225 and other medical isotopes in cleanrooms, hot cells and gloveboxes, balancing safety, quality and regulatory requirements. You’ll operate within a cGMP framework and contribute to continuous improvement of production processes.

The role requires hands-on technical work, strong documentation, and the ability to train less-experienced team members.

Formación

  • Bachelor's degree in chemistry, chemical or nuclear engineering, radiological sciences or related field.
  • Approx. 3 years of radiopharmaceutical manufacturing or regulatory environment experience preferred.
  • Experience with strict procedures, radiological controls, and recordkeeping.

Responsabilidades

  • Execute qualified production activities in a cGMP environment including chemical prep and radiopharmaceutical processing.
  • Set up and operate production equipment; manage materials, reagents, and waste.
  • Maintain clean, organized work areas and thorough production documentation.
  • Train and coach technicians and other specialists on production processes.

Conocimientos

Chemistry/Engineering degree
3+ years radiopharm
Disciplined procedures
Technical reasoning
Technical writing
Analytical skills
Train and coach others
Radiological safety
Flexible schedule

Educación

Chemistry/Engineering degree

Herramientas

Gloveboxes

Descripción del empleo

TerraPower Isotopes is seeking a Radioisotopes Production Specialist to produce actinium-225 and other medical isotopes in cleanrooms, hot cells and gloveboxes, balancing safety, quality and regulatory requirements. You’ll operate within a cGMP framework and contribute to continuous improvement of production processes.

The role requires hands-on technical work, strong documentation, and the ability to train less-experienced team members.

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