Company Profile

Job DescriptionKickstart Your Career at Vertex!Are you ready to make a real impact? At Vertex, our mission is to tackle serious diseases and to change lives, for the better, for the future. Our aim is to give you the skills, insights, and career guidance to be an important part of that future; to turn your potential into progression. As a Vertex intern or co-op, you'll work on meaningful projects, collaborate with talented teams, and learn from industry leaders. We're passionate about innovation, ...

Job DescriptionVertex currently operates at the forefront of rare disease scientific innovation and has successfully developed and commercialized multiple breakthrough medicines for Cystic Fibrosis (CF). In addition to clinical development programs in CF, Vertex has more than a dozen ongoing research programs focused on the underlying mechanisms of other serious diseases including programs in Type 1 diabetes, hemoglobinopathies, APOL-1 Mediated Kidney Disease (AMKD), Duchenne Muscular Dystrophy, ...

Job DescriptionGeneral Summary:The Senior Director, Clinical Pharmacology will serve as a Disease Area leader for Clinical Pharmacology. The Senior Director, Clinical Pharmacology will also manage the scientific functions and coordinate the activities of the Clinical Pharmacology function in collaboration with the other Disease Area leaders. The role's responsibilities will include maintaining organizational processes across the group, influencing clinical program strategy, and integrating ...

Job DescriptionPrincipal Cloud Infrastructure EngineerLocation:Boston, MA (Vertex Headquarters) Position SummaryThe Principal Cloud Infrastructure Engineer will lead the design, implementation, and optimization of enterprise-scale Azure cloud infrastructure with a strong emphasis on automation, operational excellence, and emerging AI technologies. This role will serve as a technical leader responsible for architecting resilient, scalable, and secure cloud solutions that support critical business ...

Job DescriptionJob TitleDirector, Medical Affairs - Pain DepartmentMedical Affairs LocationBoston, MA, United States General SummaryThe Director, Medical Affairs - Pain will provide strategic medical leadership and oversees the development and execution of medical strategies and plans for acute pain management in the U.S. region under the guidance of the Senior Medical Director. This role will focus on fostering scientific exchange, supporting evidence generation and scientific communications, ...

Job DescriptionThe Product Quality Associate Director is accountable for end-to-end quality oversight of small molecule program(s) throughout clinical development, commercialization, filing, approval, launch, and post-approval lifecycle management activities. This oversight includes setting and maintaining overall Quality strategies in support of commercialization efforts including establishing relevant product quality standards for current or novel technologies (including devices where applicable), ...

Job DescriptionAs the Associate Director of Sales Planning and Incentive Compensationyou will be responsible for the administration, execution, and delivery of our Sales Planning & Incentive Compensation (IC) services for the US Kidney sales team. This includes the sales team alignments, targeting, and incentive compensation deliverables. You will be a strong collaborator with the business unit teams to proactively recommend sales planning and IC strategy to ensure alignment with brand objectives, ...

Job DescriptionGeneral Summary:The Quality Manager is a technical resource in the principles and application of quality assurance and compliance. This position performs and leads activities "on the floor" in support of batch records review and disposition while ensuring compliance with cGMPs policies and procedures. The Quality Manager coordinates or executes activities on a wide range of projects and takes a role in the design and execution of new projects. Key Duties and Responsibilities:Collaborate ...

Job DescriptionGeneral Summary:The Quality Manager is a technical resource in the principles and application of quality assurance and compliance. The Quality Manager coordinates or executes activities on a wide range of projects and takes a role in the design and execution of new projects. The role will also have responsibilities associated with QC data review for both non-routine and routine cGMP process testing and in support of stability testing of Cell & Genetic Therapy products. This role ...

Job DescriptionGeneral Summary:The Associate Director, GMP Operational Quality is responsible for quality oversight of QC data review for both non-routine and routine cGMP process testing and in support of stability testing of Cell & Genetic Therapy products. The role will also oversee team activities, development of personnel and ensuring quality of deliverables within department purview. The incumbent has comprehensive knowledge of principles and application of quality assurance and compliance. ...