Stability Associate — GMP & Regulatory Submissions

A leading staffing firm is seeking a Stability Associate for a 6-month temporary role in Waltham, MA. The position involves managing GMP stability programs, ensuring compliance with ICH and FDA guidelines, and authoring stability reports. A BS or MS in science and at least 2 years of related experience in the pharmaceutical industry are required. Strong analytical and communication skills are essential, along with proficiency in Microsoft Office and SAS JMP.
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