Associate Director, GMP QA - Analytical Biologics

Job Description The role is recognized as an expert internally in the principles and application of quality and regulatory compliance. The individual adapts to new and multiple projects, effectively ensuring alignment with corporate goals and compliance with all regulatory requirements. This role is responsible for managing compliance data review in support of biologics development programs at Vertex. The role is also responsible for coordinating with Quality Disposition teams for review of development program product release testing and Certificate of Analysis approval. This role will manage direct reports to execute the team’s responsibilities. This position reports to Director, GMP Operations Quality. This role requires a minimum of 3 days onsite per week at our Boston, MA office .…