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Advisor / Sr. Advisor - Analytical Development And Quality Control
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- Avid Radiopharmaceuticals, Inc. (Avid RP), a wholly-owned subsidiary of Eli Lilly and Company, is a molecular imaging company developing diagnostics and biomarkers that improve global health by accelerating the development of new medicines and enabling a tailored approach to healthcare.
- The Advisor/Technical Lead is responsible for providing technical expertise and leadership to independently contribute to all aspects of analytical development within the Analytical Development and Quality Control group in support of Avid’s drug development program.
- Responsibilities: Provide scientific leadership throughout the Analytical Development and Quality Control group and acquire new analytical knowledge and capabilities that are needed to support novel research projects.
- Build a diverse cross-functional internal network and stay current with external scientific developments related to both analytical chemistry and radiopharmaceuticals and share knowledge with the Analytical Development and Quality Control group.
- Provide on-site support for studies at CMO sites within the US and internationally (e.g. analytical technology transfer, stability studies, studies contracted to CRO’s) as required and provide troubleshooting support for analytical method or drug product issues, as needed.
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