Atrium Works

Job DescriptionThe Process Dev Engineering Senior Scientific Associate will be part of a team that will support cell therapy scaleup process development including performing process optimization activities as well as the characterization of cell products for ongoing and future project More...

Job DescriptionGeneral Summary:The Business Systems Senior Analyst supports commercialofftheshelf (COTS) and straightforward custom solutions in support of their department. The Business Systems Senior Analyst will partner with business leadership & project managers to deliver cap More...

Job DescriptionGeneral Summary:The Pathology Research Associate will perform routine and specialized histology techniques wet lab work data acquisition and compilation using stateoftheart molecular pathology techniques. The incumbent will interface closely with other scientists veteri More...

Job DescriptionThe Quality Senior Specialist role will work with the GDP Operational QA Management team to ensure that medicines are distributed in the USA in compliance with GDP and GMP requirements. The Quality Senior Specialist will manage the daytoday Quality oversight of the Thir More...

Job DescriptionThe GMP Operational Quality Senior Specialist Contractor supports the principles and application of quality assurance and regulatory compliance. The incumbent supports or executes a wide range of activities and supports new/existing project initiatives. The GMP Operatio More...

Job DescriptionThe cell and gene analytical technologies team (CGAT) within Vertex cell and genetic therapies (VCGT) is seeking an individual for 12month contract who is able to: Work on a WednesdaySunday schedule and flexible to work in both locations of Vertex buildings within 1.0mi More...

Job DescriptionThe Sr. Quality Specialist is recognized as an expert internally in the principles and application of quality assurance and compliance. The Sr. Quality Specialist coordinates GMP activities in support of clinical and commercial Drug Product disposition. This position re More...

Job DescriptionThe Logistics (Shipping) Validation Engineer / Specialist will be responsible for overseeing and supporting the creation and management of logistics related validation records such as Operational Qualification (OQ) Performance Qualification (PQ) documents as well as sup More...

Job DescriptionThe Process Development Engineering Scientific Associate will be part of a team that will support cell therapy scaleup process development including performing process optimization activities as well as the characterization of cell products for ongoing and future projec More...

Job DescriptionGeneral Summary:The Onboarding Coordinator is responsible for establishing a best in class prehire experience for new hires. This role is also responsible for ensuring quality management and fulfillment of HR Service requests. In this role the incumbent will develop bro More...

Job DescriptionThe Advertising Promotion Associate Director is responsible for providing strategic and tactical regulatory support and guidance for assigned product and disease state communications for Vertex product(s) and/or development program(s). This role works with crossfunction More...

Job DescriptionThe Commercial Supply Chain Coordinator is responsible for straightforward administrative activities within Commercial Supply Chain; activities typically consist of welldefined support tasks that are performed under moderate supervision.Key Duties & Responsibilities More...

Job DescriptionThe Senior Specialist is recognized as having a functional knowledge in the principles and applicationofqualityassuranceandregulatorycompliance.TheSenior Specialist ensurestimelydeliveryof activities to support developmental programs.The Senior Specialist supports or ex More...

Job DescriptionAnalytical Chemistry Research Scientist ContractorJob DescriptionVertex is seeking a highly motivated analytical chemist to provide commercial product analytical support. You will work directly with our contract manufacturing organizations and a highly diverse group of More...

Job DescriptionThe Medical Affairs Associate Director (T1D) is a key role in Global Medical Affairs working on global activities for a designated disease area(s). Key responsibilities include but are not limited to Medical Plan development launch strategy and scientific leadership ex More...

Job DescriptionThis position will be within the Engineering and Materials Science department which supports Vertexs drug development programs by developing a deep understanding of the relationships between materials properties pharmaceutical processing conditions and final product per More...

Job DescriptionThe Sr. Quality Specialist Compliance is recognized as an expert internally in the principles and application of quality assurance and compliance. The Sr. Quality Specialist will coordinate GMP activities in support of clinical and commercial Drug Product disposition. More...