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Celldex will make every effort to respond to inquiries from qualified applicants who have the skills and interests we are seeking. We will not be able to respond to recruiting and placement firms who contact us in an unsolicited manner, nor to unqualified applicants. Celldex is an equal opportunity employer dedicated to diversity in the workplace.
The Assistant / Associate Scientist - Analytical Development (AD) will be responsible for providing analytical support to Quality Control (QC). This includes, but is not limited to, the following: development of new analytical methods for QC, overseeing transfer of new methods from AD and Research & Development to QC; troubleshooting problems with existing QC methods; qualification of new reference materials, controls, and critical reagents; biochemical characterization testing of cGMP and developmental product manufactured by Celldex Biomanufacturing Operations, as well as drafting Technical Reports for development, qualification and characterization analyses performed.
The scientist will design, execute, analyze and interpret experiments using in-vitro and ex-vivo assays to support antibody discovery, lead identification and characterization, and translational research efforts for clinical development candidates.
As a Quality Control (QC) Analyst III at Celldex Therapeutics, you’ll be responsible for everything associated with routine and non-routine lab work assigned by departmental management at our Fall River MA facility.
If you have laboratory experience in the biotechnology / pharmaceutical industry and want to work in a collaborative small team environment with a great group, this is an opportunity you’ll want to explore!
Celldex Therapeutics, Inc. is developing a pipeline of immunotherapy and targeted cancer therapies. We are conducting clinical trials across multiple product candidates.