Lead the development and implementation of continuous improvement quality operations activities and processes. Ensure Quality Operations processes are in compliance with regulations. Proactively identify gaps and mitigate risks. Lead/Participate in development the strategy for project and represent as the quality expert in governance forums to ensure Quality requirements

The Senior Director, Quality GLP, Biomarkers and Research has overall accountability for strategic leadership and oversight of the end to end quality assurance strategy for proactive, risk informed, and sustainable quality oversight and compliance with regulatory expectations across Vertex processes for clinical evidence generation and product vigilance Key Duties and Res

Vertex is seeking a talented and motivated individual with the desire to be part of a highly innovative company aimed at transforming the lives of people with serious diseases, their families and society. The role is as an Associate Director within the Modeling Center of Excellence (CoE), a designated group within the HEOR team that provides strategic and technical modeli

Develop and implement data driven insights and analytics strategies to support market access decisions and GTN optimization. Drive the development of GTN models, forecasting accuracy, and scenario analysis to support pricing decisions and revenue projections for LE and LRP processes. Provide strategic guidance and recommendations to senior leadership based on comprehensiv

Reporting to the Director of Revenue Financial Planning and Analysis, the Senior Manager of Revenue FP&A is a key member of Vertex's Commercial Finance team, partnering closely with N orth America and Global Commercial teams to report key metrics and provide financial insights . Th e candidate will play a key role in global business partnering with multiple functions on t

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

The Trade and Distribution Data Analytics Manager will be responsible for supporting insights activities. The insights are used to track business performance and provide key data to inform business decisions. The Manager will typically partner with their manager on key projects and will be responsible for running market research or data analysis. This is a hybrid/on site

Define, plan and execute the full scope of assigned projects. Ability and willingness to perform project tasks at all levels to meet the project needs, from basic to complex, both independently and collaboratively Identify, analyze, prioritize, communicate and mitigate project risks Manage multiple projects simultaneously to successful outcomes Forecast, track and manage

The Principal Biostatistician will perform advanced scientific statistical analyses in support of the company's Global Medicines Development and Affairs area with some guidance and mentoring on new and complex issues. The incumbent will completed work in a resourceful, self sufficient manner and create alternative approaches to achieve desired results. The incumbent shoul

Vertex has established a new research site in Boston Seaport where research, development, and clinical manufacturing for cell and genetic therapies will be primarily based. Cell and genetic therapies represent two rapidly emerging therapeutic modalities with the potential to treat and even cure several of the diseases Vertex is focused on, including sickle cell disease, D

The GMP Quality Operations Director serves as a Quality leader in the areas of process validation, and equipment validation in oral solid dosage form. The Director is also responsible for managing multiple department activities with a high degree of independence while providing oversight of the development, implementation, and maintenance of relevant quality initiatives i

The Training Associate Director is responsible for supporting the oversight of all Training related activities within the Global Regulatory Affairs organization. This role will work to create, curate, and deliver top notch learning experiences including both technical and professional development for the team. The Training Associate Director will report directly to the Se

The Director, Modeling & Simulations (M&S) Pharmacometrics will be responsible forindependently determining, planning, and executing M&S analyses for an entire drug development program in close collaboration with cross functional colleagues within the R&D organization. In this role, it is expected that the incumbent will represent M&S with cross functional drug developmen

Build and manage a manufacturing engineering team for DSDP cells and combination products Act as primary technical and engineering manufacturing lead design reviews, documentation with focus on designing for manufacturability. Implement, propose and drive the implementation of Drug Product Device and manufacturing engineering controls by integrating Vertex QMS, production

Provides comprehensive expertise and guidance in designated therapeutic area(s) and Vertex medicines Leads a team of physicians and scientists to create and execute appropriate medical affairs plans and tactics supporting designated therapeutic area(s) and Vertex medicines Develops and maintains professional relationships with local Health Care Professionals, and with loc