A biotechnology firm in Waltham, MA seeks an Associate Director of Quality Control to lead strategic activities related to analytical methods for clinical trial materials. The ideal candidate will have over 10 years of experience in a cGMP environment, managing QC activities, and ensuring compliance with regulatory standards. This role also involves collaboration with cross-functional teams and oversight of external partners. A strong background in analytical methods and excellent communication skills are essential. Target salary range is $176,400 - $215,600.
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