PET Radiochemist
About The Position
The PET Radiochemist is responsible for the daily production and quality control of routine PET drugs. The PET RC assists in the synthesis of PET radiopharmaceuticals for clinical and research studies. The PET Radiochemist will also be responsible for completing and maintaining the appropriate documentation required by federal and state agencies associated with the production and distribution of the PET drug product/radioisotopes. The PET Radiochemist will help in set up and maintain automated chemistry modules and other laboratory equipment and the development of synthesis procedures in the production of PET radiopharmaceuticals/radioisotopes and will provide instruction and training to other radiochemistry staff as needed. PET Radiochemist – quality control: Responsible for daily quality control of routine PET drug products Responsible for setup and use of analytical chemistry equipment Responsible for assessing suitability of incoming materials Responsible for determining acceptability of productions for release Responsible for retrospective testing on productions post-release Responsible for quality control method validation and post repair instrument verification. PET Radiochemist – quality assurance: Responsible for qualification and monitoring of all vendors and suppliers. Responsible for the accuracy and upkeep of documentation used in all aspects of the facility Responsible for ensuring adequate training of all PET Radiochemists Responsible for conducting regular internal audits and self-inspections Involved in deviation/OOS and CAPA investigations Reviews and approves change control events and processes.
Requirements
- Requires a Bachelor’s degree in chemistry, nuclear medicine technology, pharmacy or related field.
- Experience in handling PET radiopharmaceuticals/radioisotopes working with radioactivity such as in a PET radiochemistry lab, nuclear medicine environment, or commercial nuclear chemistry laboratory specializing in PET radioisotope production.
- Basic Life Support Certification is required upon hire and must be valid for 90 days or greater from start date.
Nice To Haves
- Experience in helping develop synthesis procedures is preferred.
- Candidate should have strong skills in teaching and training, and with group interaction and presentations.
Responsibilities
- daily production and quality control of routine PET drugs
- assists in the synthesis of PET radiopharmaceuticals for clinical and research studies
- completing and maintaining the appropriate documentation required by federal and state agencies associated with the production and distribution of the PET drug product/radioisotopes
- help in set up and maintain automated chemistry modules and other laboratory equipment and the development of synthesis procedures in the production of PET radiopharmaceuticals/radioisotopes
- provide instruction and training to other radiochemistry staff as needed
- daily quality control of routine PET drug products
- setup and use of analytical chemistry equipment
- assessing suitability of incoming materials
- determining acceptability of productions for release
- retrospective testing on productions post-release
- quality control method validation and post repair instrument verification
- qualification and monitoring of all vendors and suppliers
- accuracy and upkeep of documentation used in all aspects of the facility
- ensuring adequate training of all PET Radiochemists
- conducting regular internal audits and self-inspections
- involved in deviation/OOS and CAPA investigations
- reviews and approves change control events and processes
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
