Full time
Vertex Pharmaceuticals
Boston, MA, USA
Job Description General Summary: The Manufacturing Process & Technical Quality Associate Director is accountable for end-to-end technical quality oversight of cell and genetic program throughout clinical development, commercialization, product launch and post approval lifecycle management activities. This includes establishing relevant product quality standards for current or novel technologies, ensuring internal and cross-functional alignment with industry and regulatory expectations, and identifying product quality risks and mitigations throughout development for the assigned programs. The role will closely partner with operational stakeholders to participate in Cell & Genetic therapies projects and associated governance to meet business, regulatory and operational requirements. Key Duties and Responsibilities: Lead and/or participate in the development and implementation of Quality compliance principles throughout product lifecycle management within...

