Sr. Associate II - Method Validation - Indianapolis, IN

, ATTENTION MILITARY AFFILIATED JOB SEEKERS, - Our organization works with partner companies to source qualified talent for their open roles. The following position is available to, Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers. If you have the required skill set, education requirements, and experience, please click the submit button and follow the next steps. Unless specifically stated otherwise, this role is 'On-Site' at the location detailed in the job post., At RayzeBio, every day is an opportunity to ignite meaningful change. As a wholly-owned subsidiary of Bristol Myers Squibb, RayzeBio blends the nimble, pioneering spirit of an emergent biotech with the global expertise and resources of a leading innovator in oncology. Our mission is to develop transformative radiopharmaceutical therapies that offer new hope for patients living with cancer. Here, youâll join a multidisciplinary team where your ideas are valued, your expertise is amplified, and collaboration is at the heart of everything we do. From day one, expect to make an immediate impactâ”on our science, on our teams, and most importantly, on patients., RayzeBio, a Bristol Myers Squibb company, is looking for a Senior Associate II, Analytical Development at their Indianapolis manufacturing site. The person will be responsible for method development and implementation, method validation, verifications, or transfer, as well as stability testing activities to support product development at the RayzeBio manufacturing site in Indianapolis. The Senior Associate II, Analytical Development will report directly to the Manager of Analytical Development at the Indianapolis site.Job Responsibilities:Essential duties and responsibilities include the following. , Other duties may be assigned.Develop and validate analytical methods for parenteral radiopharmaceutical products according to phase appropriate guidelines, including UHPLC, HPLC, GC, TLC, ICP, LC-MS, Gamma Spectrometry, Alpha Spectrometry, and other techniques as required.Participate in method transfer activities from CDMO or internal research facility to QC team, ensuring accuracy and reliability of data.Prepare analytical test methods and method validation, verification, and transfer protocols and reports in accordance with applicable guidelines and industry standards (e.g. USP, EP, and ICH).Work closely with other teams to ensure timely delivery of analytical results and support product development and commercialization.Participate in troubleshooting and investigations of analytical issues, identify root causes, and implement corrective actions.Develop and maintain appropriate documentation, including notebooks, protocols, reports, standard operating procedures and associated forms, and data analysis.Participate in instrument qualification, calibration, and maintenance activities.Ensure compliance with GMP regulations, safety guidelines, and quality standards.Work with RSO to ensure laboratory compliance with the radiation safety programs.Provide technical support to other teams or business units as required.Source and on-board analytical technologies as required.Perform other duties as required by management.The position is salaried. , Work will be predominantly first shift, M-F, but extended hours or weekend work based on radiopharmaceutical manufacturing schedule may be required., This position will require the applicant to work with and around ionizing radiation and hazardous chemicals. , , , , , ,

Created: 2026-02-23