Description
The Associate Director of Quality will manage quality assurance activities, oversee the implementation of a Quality Management System, and ensure compliance with FDA, ICH, GLP, GMP, and GCP requirements across CROs and CDMO partnerships. The role includes developing quality systems and SOPs, managing CRO oversight and vendor relationships, maintaining documentation and change control, and leading quality initiatives from preclinical research through clinical development. It is a full-time hybrid position requiring a life sciences or related bachelor’s degree, at least 10 years of biotech experience, and 3–5 years managing CROs and vendor relationships.
