Radiopharmaceutical Chemist
University of ChicagoAbout the role
Department
BSD RAD - Cyclotron
About the Department
Job Summary
For the position that we are considering, the applicant needs to have skills in 1) synthetic chemistry, pharmaceutical or radiopharmaceutical research and production, 2) analytical techniques for molecular characterization and quality control, 3) experience in working in high levels of radiation and with large amounts of radioactivity is very desirable, but not required, and 4) and clear ability to work in a complex, sometimes high-stress, and multiple-worker environment, for example, a pharmaceutical production facility would all be appropriate, and 5) ability to write research reports, develop and follow Standard Operating Procedures.
Primary functions of this role include but are not limited to develop and validate processes for producing radiopharmaceuticals following appropriate regulatory guidelines, including synthesis, purification, formulation, and quality control, contribute to developing novel radiotracers and radiopharmaceuticals for molecular imaging and therapy, including radiotheranostics, participates in maintaining the radiopharmaceutical facility for regulatory compliance, and also contributes to direct quality control analysis of final radiopharmaceutical products. Additionally, our ideal candidate must also be able to work with large quantities of radioactivity and in radiation environments with appropriate radiation safety precautions.
Responsibilities
Production of established and new radiopharmaceuticals for preclinical and human use. Includes preparation of solvents, reagents, and ancillaries required for the synthesis and QC.
Support various research projects involving imaging and/or therapeutic radionuclides, and radiolabeling of small molecules, peptides, and biologicals. Includes radiochemical processing of various radiometals and subsequent radiolabeling of desired molecules.
Performs work with (not all are required) aseptic procedures, microbiological procedures, handling of highly radioactive pharmaceutical products, DOT procedure.
Writes, proofreads, and develops Chemistry, Manufacturing and Controls (CMC); Standard Operating Procedures (SOPs) if necessary.
Oversees maintenance and production schedules with the accelerator and its subsystems, running the machine on an intermittent basis.
Uses subject matter and best practices knowledge to perform lab and/or research-related duties and tasks. Works independently to assist with project design.
Solves complex problems relating to the administration of projects, including planning new procedures, adapting existing procedures to the needs of the project, and making significant contributions to methodology.
Performs other related work as needed.
Minimum Qualifications
Education:
Minimum requirements include a college or university degree in related field.
Work Experience:
Certifications:
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Preferred Qualifications
Education:
Master’s degree in a related field.
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