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Job DescriptionThe Sr. Quality Manager is an advanced technical resource in the principles and application of quality assurance and compliance. The Sr. Quality Manager coordinates or executes activities on multiple complex projects with emphasis on QA GMP disposition of drug products
Job DescriptionThe Sr. Quality Manager is an advanced technical resource in the principles and application of quality assurance and compliance. The Sr. Quality Manager coordinates or executes activities on multiple complex projects with emphasis on QA GMP disposition of drug products
Job DescriptionThe Sr. Quality Manager is an advanced technical resource in the principles and application of quality assurance and compliance. The Sr. Quality Manager coordinates or executes activities on multiple complex projects with emphasis on QA GMP disposition of drug products
Job DescriptionThe Sr. Quality Manager is an advanced technical resource in the principles and application of quality assurance and compliance. The Sr. Quality Manager coordinates or executes activities on multiple complex projects with emphasis on QA GMP disposition of drug products
Job DescriptionThe GMP QA Analytical Sr. Quality Specialist recognized as a subject matter expert in the principles and application of quality assurance and compliance in support of QA Analytical function. The Sr. Quality Specialist supports and executes wide range of activities relat
Job DescriptionThe GMP QA Analytical Sr. Quality Specialist recognized as a subject matter expert in the principles and application of quality assurance and compliance in support of QA Analytical function. The Sr. Quality Specialist supports and executes wide range of activities relat
Job DescriptionThis 2nd shift staff member on the MTO is responsible for ownership and execution of quality records including Deviations CAPAs Change Controls and Analytical and Quality Control Investigations supporting cell manufacturing at our Boston site. This includes all aspects
Job DescriptionThis 2nd shift staff member on the MTO is responsible for ownership and execution of quality records including Deviations CAPAs Change Controls and Analytical and Quality Control Investigations supporting cell manufacturing at our Boston site. This includes all aspects
Job DescriptionThe Vertex Cell and Gene Therapy (C>) Quality Control (QC) team is responsible for the routine testing of samples and associated workflows for our internally manufactured stem-cell based T1D and genetically modified Casgevy programs. C> QC carries out all activities
Job DescriptionThe Vertex Cell and Gene Therapy (C>) Quality Control (QC) team is responsible for the routine testing of samples and associated workflows for our internally manufactured stem-cell based T1D and genetically modified Casgevy programs. C> QC carries out all activities
Job DescriptionThe Vertex Cell and Gene Therapy (C>) Quality Control (QC) team is responsible for the routine testing of samples and associated workflows for our internally manufactured stem-cell based T1D and genetically modified Casgevy programs. C> QC carries out all activities
Job DescriptionThe Vertex Cell and Gene Therapy (C>) Quality Control (QC) team is responsible for the routine testing of samples and associated workflows for our internally manufactured stem-cell based T1D and genetically modified Casgevy programs. C> QC carries out all activities
Job DescriptionThe Process Dev Engineering Technician will be part of a team that supports cell therapy media development and scale up working with the media and factor preparation teams to ensure components are prepared with high consistency and accuracy.Key Duties and Responsibiliti
Job DescriptionThe Process Dev Engineering Technician will be part of a team that supports cell therapy media development and scale up working with the media and factor preparation teams to ensure components are prepared with high consistency and accuracy.Key Duties and Responsibiliti
Atrium Works
Job DescriptionScientist Analytical DevelopmentPosition SummaryWe are seeking a talented and highly motivated (Scientist) Analytical Development to support analytical strategy and method development for complex therapeutic programs with an emphasis on biologics and cell and gene thera
Job DescriptionScientist Analytical DevelopmentPosition SummaryWe are seeking a talented and highly motivated (Scientist) Analytical Development to support analytical strategy and method development for complex therapeutic programs with an emphasis on biologics and cell and gene thera
Job DescriptionThis staff member on the MTO is responsible for ownership and execution of quality records including Deviations CAPAs Change Controls and Analytical and Quality Control Investigations supporting cell manufacturing at our Boston site. This includes all aspects of QE exec
Job DescriptionThis staff member on the MTO is responsible for ownership and execution of quality records including Deviations CAPAs Change Controls and Analytical and Quality Control Investigations supporting cell manufacturing at our Boston site. This includes all aspects of QE exec
Job DescriptionManager Analytical Science & Technology (ASAT) will support analytical lifecycle management activities for commercial Cell and Gene Therapy (CGT) products within the Commercial Manufacturing & Supply Chain (CMSC) organization. This role will focus on analytical data ver
Job DescriptionManager Analytical Science & Technology (ASAT) will support analytical lifecycle management activities for commercial Cell and Gene Therapy (CGT) products within the Commercial Manufacturing & Supply Chain (CMSC) organization. This role will focus on analytical data ver
Job DescriptionSpecialist Analytical Science & Technology (ASAT) will support analytical lifecycle management activities for commercial Cell and Gene Therapy (CGT) products within the Commercial Manufacturing & Supply Chain (CMSC) organization. This role will focus on analytical data
Job DescriptionSpecialist Analytical Science & Technology (ASAT) will support analytical lifecycle management activities for commercial Cell and Gene Therapy (CGT) products within the Commercial Manufacturing & Supply Chain (CMSC) organization. This role will focus on analytical data
Job DescriptionRole/Title: VMC Operational Excellence Project ManagerW2Full time on site in Boston12 month contractProposed Role & Responsibilities:Operational Excellence and Process ImprovementLead process discovery and assessment activities across manufacturing and business operatio
Job DescriptionRole/Title: VMC Operational Excellence Project ManagerW2Full time on site in Boston12 month contractProposed Role & Responsibilities:Operational Excellence and Process ImprovementLead process discovery and assessment activities across manufacturing and business operatio
Job DescriptionRole/Title: VMC Operational Excellence Project ManagerW2Full time on site in Boston12 month contractProposed Role & Responsibilities:Operational Excellence and Process ImprovementLead process discovery and assessment activities across manufacturing and business operatio
Job DescriptionRole/Title: VMC Operational Excellence Project ManagerW2Full time on site in Boston12 month contractProposed Role & Responsibilities:Operational Excellence and Process ImprovementLead process discovery and assessment activities across manufacturing and business operatio
Job DescriptionMSAT Lifecycle Management Data & Process Specialist executes the completeness validation and delivery of commercial manufacturing data for the Manufacturing Science and Technology (MSAT) department throughout the commercial product lifecycle. Operating within the Lifecy
Job DescriptionMSAT Lifecycle Management Data & Process Specialist executes the completeness validation and delivery of commercial manufacturing data for the Manufacturing Science and Technology (MSAT) department throughout the commercial product lifecycle. Operating within the Lifecy
Job DescriptionThe Senior Quality Specialist (2nd Shift) is recognized as an expert 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 disp
Job DescriptionThe Senior Quality Specialist (2nd Shift) is recognized as an expert 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 disp
Atrium Works
Job DescriptionTheSr. AdministrativeAssistant plays an important role in ensuring the effective and efficient maintenance of departmentalprocesses proceduresandprograms inclusive of calendar management scheduling vendormeetingstravel arrangementsandexpenses. It is imperative this pers
Job DescriptionTheSr. AdministrativeAssistant plays an important role in ensuring the effective and efficient maintenance of departmentalprocesses proceduresandprograms inclusive of calendar management scheduling vendormeetingstravel arrangementsandexpenses. It is imperative this pers
Job DescriptionJob DescriptionThe Analytical Development Principal Research Associate performs and supports analytical method development activities for cell therapy products and other biologics. In this on-site role you will perform laboratory-based experiments execute sample testing
Job DescriptionJob DescriptionThe Analytical Development Principal Research Associate performs and supports analytical method development activities for cell therapy products and other biologics. In this on-site role you will perform laboratory-based experiments execute sample testing
Job DescriptionJob DescriptionThe Analytical Development Principal Research Associate performs and supports analytical method development activities for cell therapy products and other biologics. In this on-site role you will perform laboratory-based experiments execute sample testing
Job DescriptionJob DescriptionThe Analytical Development Principal Research Associate performs and supports analytical method development activities for cell therapy products and other biologics. In this on-site role you will perform laboratory-based experiments execute sample testing
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
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
Job DescriptionThe Cell and Gene Therapy Process Development team at Vertex Pharmaceuticals is seeking candidates to help evaluate design and implement robust enterprise-level data pipeline solutions that streamline data flow from generation to analysis which will accelerate process u
Job DescriptionThe Cell and Gene Therapy Process Development team at Vertex Pharmaceuticals is seeking candidates to help evaluate design and implement robust enterprise-level data pipeline solutions that streamline data flow from generation to analysis which will accelerate process u
