Seeking a scientist to perform analytical testing for biologic product release and characterization in a cGMP/GLP environment. Responsibilities include routine testing, documentation, troubleshooting HPLC/UPLC/CE methods, and ensuring compliance.Responsibilities Include: 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, iCE, cIEF, CE-SDS, Titer, Peptide, and Glycan mapping - 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.
- ID: #53788274
- State: Massachusetts Lexington 02420 Lexington USA
- City: Lexington
- Salary: USD TBD TBD
- Job type: Full-time
- Showed: 2025-04-11
- Deadline: 2025-06-10
- Category: Et cetera