Overview: The Analytical Scientist is responsible for developing and validating analytical methods for a variety of radioligand therapy (RLT) products for our clients in the Nucleus RadioPharma radiopharmaceutical development laboratory. PRINCIPAL RESPONSIBILITIES: Develop and validate GMP-compliant analytical methods for a variety of radiopharmaceutical drug products using HPLC, TLC, GC, gamma spectroscopy, endotoxin testing, pH, etc. Lead the technical execution of analytical development activities at the Rochester site. Work with development team to generate the required CMC data package for the client. Help build technical expertise to meet future radiopharmaceutical drug product needs. Assist the development team in building project plans, timelines, and reports for the client. Work closely with scientific staff to evaluate technical feasibility of new products. Work with QC team in transferring analytical procedures to QC laboratory. Order materials for analytical work, oversee analytical instruments in the development laboratory and support laboratory operation for instrument qualification. Record experiments and test results accurately to meet corporate requirements. Draft development reports, validation protocols and SOPs for test methods. Perform other duties as assigned.