The Senior Quality Specialist is recognized as an expert internally in the principles and application of quality assurance and compliance. The Senior Quality Specialist coordinates GMP activities in support of clinical and commercial Drug Product manufacturing and disposition. This is an on site position on the 2nd shift. KEY DUTIES AND RESPONSIBILITIES Review batch data,

Vertex Pharmaceuticals Inc. has established a state of the art GMP manufacturing facility in Boston less than a mile from the Corporate Headquarters in the Seaport District. This GMP facility is a keystone to delivering our strategy of bringing transformative medicines to patients in need, from clinical development to commercialization. The Senior Specialist will be respo

Identify and develop technical solutions to enable program and company goals. Contribute to the design and implementation of efficient and scalable manufacturing processes for commercial application, working closely with cross functional teams including process development, manufacturing, and engineering. The role includes the design and execution of process scale up stra

Responsibility Researches and presents recommendations to management on software and hardware required to develop a totally computer controlled manufacturing environment. Integrates Robotic systems, machinery controls and computer networks into operating system. Using available technology provides integration with video systems for use in quality control, safety devices,