• Synthesis of Radiolabeled Compounds: Design, synthesize, and optimize radiolabeling methods of compounds (e.g., PET, SPECT, and alpha emitting isotopes) for use in preclinical and clinical studies.
• Radiochemical Purity and Quality Control: Perform and develop analytical methods to ensure the radiochemical purity, stability, and quality of radiolabeled compounds. Contribute to the development of critical quality attributes of various products.
• Process Development: Contribute to the development and optimization of radiolabeling processes through identification of critical process parameters, including scale-up for clinical production.
• Regulatory Compliance: Ensure all radiochemical activities comply with relevant regulations, including GMP, GLP, and safety protocols.
• Documentation: Maintain accurate records of all experiments, procedures, and results. Prepare technical reports and contribute to regulatory submissions.
• Cross-Functional Collaboration: Work closely with other departments, including Manufacturing, Pharmacology, and Clinical Development, to support the integration of radiochemistry into the drug development process.
• Safety: Uphold strict safety standards in handling radioactive materials and participate in the maintenance of radiation safety procedures and protocols.
• Innovation: Stay abreast of the latest advancements in radiochemistry and radiopharmaceutical development and apply this knowledge to drive innovation within the company.

Education/Experience               

• Education: Ph.D. in Radiochemistry, Chemistry, or a related field. Exceptional candidates with a Master’s degree and significant experience will also be considered.
• Experience: 3+ years of experience in radiochemistry, preferably in a pharmaceutical or clinical research environment.
• Proficiency in the synthesis and handling of radioactive isotopes (e.g., Pb-203, Pb-212, Ga-68, Cu-64, Cu-67 and F-18).
• Strong background in analytical techniques such as HPLC, TLC, GC, NMR, and mass spectrometry.
• Experience with automated radiochemistry synthesis modules is a plus.
• Thorough understanding of radiopharmaceutical development, including regulatory requirements for use of products in clinical trials (e.g., 21CFR Part 211, 21CFR Part 212, etc.).

• Deep understanding of radiochemistry techniques related to the radiolabeling of molecules and their purification
• Knowledge of radioactive decay, RAM transportation regulations and international shipments
• Effective communication, including writing, speaking and interpersonal communication.
• Rapid critical thinking and problem-solving abilities.
• Excellent customer service and client relations skills.
• Organizational and time management skills.
• Great collaboration and teamwork abilities.
• Great leadership skills.
• Adaptable to work in a fast-paced environment.
• Advanced data analysis and data visualization.
• Expert inventory management.
• Ability to use computers, software and other technology for inventory and communication purposes.
• Understanding of the supply chain, including common obstacles and effective solutions.
• Flexibility to work various shifts as required.
• Flexible and willing to perform other tasks as assigned.
• Ability to lift 50 lbs. 

Work Environment 

• Must be willing to work in a facility producing radioactive materials and requiring all employees to participate in safety programs designed to minimize potential and/or actual exposure levels.
• Must be able to work outside of regular work hours, including off shift, weekend, and holiday work as business needs require.
• May be required to sit or stand for long periods of 8+ hours a day while performing duties. 
• Occasional kneeling, crouching, twisting the upper body, bending, stooping, pushing, pulling, or reaching may be required.
• Must possess good hand-eye coordination; close attention to detail is required.
• Must be able to work indoors and outdoors with exposure to mechanical/moving parts, hazards including radioactive, corrosive, flammable and toxic material, dust, dirt, odors, and irritants.
• Must be willing to wear a variety of Personal Protective Equipment (PPE), including eye and hearing protection, as needed.
• Willingness to complete safety training within allotted timeframes, and work in a team-based environment.