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.
Requirements
- Develop and validate analytical methods for parenteral radiopharmaceutical products
- Participate in method transfer activities from CDMO or internal research facility to QC team
- Prepare analytical test methods and method validation, verification, and transfer protocols and reports
- 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
- 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
Benefits
- 401k Matching
- Generous Paid Time Off
- Health Insurance
- Dental Insurance
- Vision Insurance
- Life Insurance
