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This position will support the AQL group to meet testing demands
The candidate will perform analytical testing of clinical stage biopharmaceutical products in accordance with cGMP regulations
This will include sample testing, data analysis, data review and laboratory maintenance to support lot release and stability of clinical trial material as well as method qualification and/or technology transfer
Types of analyses to be conducted: Chromatography, Electrophoresis, Immunoassay, Physiochemical/Compendial
Prior quality control or laboratory experience in a regulated industry environment
Excellent communication (oral and written) and attention to detail
Ability to work independently and as part of a team, self-motivated, adaptability, andapositive attitude
Excellent time management/organization skills
B.S. degree with 0-1 years of experience is required
Prior experience with chromatography (SEC, IEC, RPLC), electrophoresis (cIEF, cGE), physiochemical/compendial (Appearance, pH, A280) or immunoassay (ELISA, SPR) techniques is required.
Authorization to work in the United States indefinitely without restriction or sponsorship
Position is full-time, Monday-Friday, 8:00am - 5:00pm, with overtime as needed. Candidates currently living within a commutable distance ofGaithersburg, Maryland are encouraged to apply.