Contributes as part of a team of AD scientists towards execution of various analytical methods to support biological therapeutic product release and characterization testing in a compliance-based environment. Independently performs routine testing such as but not limited to SEC, CEX, RP, P20, P80, CE (icIEF Maurice), iCE, CE-SDS (Maurice and PA800) - using established Test Methods, including associated protocol/report documentation and presentations. Conducts work in compliance with cGMP/GLP, safety and regulatory requirements. Responsible for working on other non-lab-based tasks from time to time if assigned. Demonstrate independent judgment in technique and method selection, protocol and study design and execution, data analysis and use of standard practices and procedures for a variety of problems of moderate scope and complexity to meet assigned objectives. Demonstrate HPLC, UPLC and/or CE troubleshooting capabilities.
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Job Type
Full-time
Career Level
Entry Level