Technical Manager - QA Programs & Systems

Role: Technical Manager, QA Programs & Systems at Bristol Myers Squibb's cell therapy site, owning and coordinating QA shop floor programs to ensure operational success and inspection readiness. Responsibilities include leading change controls, managing risk assessments, supporting new product introductions, overseeing training lifecycle, and representing QA in sterile process and compliance initiatives. The role requires translating governance decisions into shop-floor actions and facilitating cross-functional collaboration across Manufacturing, Quality Control, Warehouse, and MSAT. Qualifications include a bachelor's degree in a STEM field and 5+ years of cGMP experience, preferably in biotechnology, cell therapy, or regulated environments, with demonstrated ownership of quality systems and project management skills. High-value biopharma specifics involve cGMP compliance, sterile processes, and support for cell therapy manufacturing. The position reports to the Associate Director, Quality Operations, and is a site-essential onsite role based in Bothell, WA, with a focus on operational excellence and continuous compliance.