Job Description
Job Summary
This Biochemist supports multiple steps in the manufacturing of BioLegend’s regulated products within our FDA-registered cGMP facility.
Responsibilities include formulation, filling, capping, labeling, completing batch records, managing finished goods inventory (FGI), data entry, equipment maintenance, and organizing and inspecting supplies.
You will also support purification and conjugation of monoclonal antibodies using an AKTA system, as well as buffer preparation and inspection of materials entering the GMP suite.
In addition, this role includes assisting with product documentation, maintaining device history records, and working with Product Development to help transition new products into manufacturing.
The ideal candidate is a dependable team player who is organized, detail-oriented, and comfortable working in a fast-paced environment. Strong communication skills and the ability to work independently while meeting deadlines are...