Senior Associate II - Analytical Development
Bristol Myers Squibb
September 15, 2026
Full-time
On-site
Indianapolis, IN
Operations
Role: Senior Associate II in Analytical Development supporting radiopharmaceutical product development at RayzeBio's Indianapolis site. Objectives: develop, validate, transfer, and troubleshoot analytical methods to ensure quality and compliance of parenteral radiopharmaceuticals. Responsibilities: perform methods like UHPLC, HPLC, GC, ICP, LC-MS, gamma and alpha spectrometry; participate in method transfer from CMO or research labs; prepare validation and verification protocols; maintain GMP compliance and safety standards; support instrument qualification, calibration, and documentation; collaborate with cross-functional teams for timely analytical support. Requirements: B.Sc./M.Sc. in Analytical Chemistry, Pharmaceutical Sciences or related field; minimum 3 years' pharmaceutical or radiopharmaceutical industry experience, especially in analytical method development and validation; strong technical proficiency in relevant techniques; knowledge of GMP, safety protocols, and radiation safety. Preferred: radiopharmaceutical or radioactive material handling experience; GMP manufacturing familiarity; experience with parenteral products. High-Value: radiopharmaceuticals, radiochemicals, GMP, validation, method transfer, gamma/alpha spectrometry, Indianapolis location. Work setup: predominantly first shift, with potential extended hours or weekend work; working with ionizing radiation and hazardous chemicals.