Atrium Works

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 المزيد...

Job DescriptionGeneral Summary:The Temporary Data Entry Associate will be responsible for entering and validating batch records into our TIBCO systemThis is a 6 month contract.Hybrid RoleKey Duties and Responsibilities:Transcribe data from multiple sources into a single fileMaintain d المزيد...

Job DescriptionVertex is seeking a talented individual to join our process chemistry group in Boston MA. This role will support drug substance development programs at Vertex performing synthetic organic chemistry in the laboratory at a high level to design and execute syntheses of cha المزيد...

Job DescriptionThe Senior Administrative Assistant plays an important role in ensuring the effective and efficient maintenance of departmental processes procedures and programs inclusive of calendar management scheduling department meetings travel arrangements and expenses. It is impe المزيد...

Job DescriptionThe drug development and commercialization project management manager(temp) is a global role within the Biopharmaceutical Sciences Cell and Gene Therapy organization. The incumbent is expected to apply project management best practices and solve complex problems and fac المزيد...

Job DescriptionThe Validation Engineer will report to the VCGT Validation leadership or an appropriate designee to execute Commissioning Qualification and Validation activities for Vertexs Cell and Gene Therapies Facility in one of their facilities located in South Boston Cambridge or المزيد...

Job DescriptionPosting Title: Temporary Contract - Principal Research ScientistLocation: Boston MADepartment: Formulation DevelopmentThis is a PT role: 20-30 hours per week.Position Overview:Vertex Pharmaceuticals is seeking a talented scientist who can join our Formulation Developmen المزيد...

Job DescriptionWere seeking a Manager of GxP Quality Document and Records Management to cross-functionally to support the GxP documentation records management and training needs of business partners. Reporting to the Associate Director of GxP Document and Records Management this role المزيد...

Job DescriptionThe GMP Quality Specialist supports the principles and application of quality assurance and regulatory compliance. The Specialist provides support and executes routine tasks related to GMP activities.Key Duties and Responsibilities:Participates in compliance related tea المزيد...

Job DescriptionThis role will report to the Associate Director of Operations Quality and focus on the design and development of clinical and commercial Class II devices. The successful candidate will join the Quality Team and work closely with Product Development Quality Control Regul المزيد...

Job DescriptionThe GMP Operational Quality Specialist works with a high degree of independence to provide QA Analytical support for release and stability program for commercial products. The GMP Operational Quality Specialist executes routine tasks and activities in support of QA Ana المزيد...

Job DescriptionThe Process Dev Engineering Scientific Associate will be part of a team that will support cell therapy media development team including performing media optimization studies as well as prepping media and characterizing media components. This role will contribute to the المزيد...

Job DescriptionJob Summary:The Senior Scientist (contractor) will be part of Analytical Science and Technology (ASAT) team within Commercial Manufacturing & Supply Chain (CMSC) department. S/He/They will provide support with development and execution of the analytical CMC strategy المزيد...

Job DescriptionVertex is seeking a talented and highly motivated individual to join our Formulation Development group in Boston MA. We are looking for a candidate with a background in parenteral formulation development and a passion for science. The Formulation Senior Research Associa المزيد...

Job DescriptionThe Quality Manager role will work with the GDP Operational QA Management team to ensure that medicines are distributed globally in compliance with GDP and GMP requirements. The Quality Manager will manage the daytoday Quality oversight of the Third Party Logistics prov المزيد...

Job DescriptionThe Senior Quality Specialist will provide QA support for commissioning Qualification and Validation (CQV) and projectrelated QA activities at Vertex Manufacturing Center (VMC) Boston MA. As a key member of our Quality Assurance team this person will be responsible for المزيد...

Job DescriptionThe key responsibilities that the candidate will be focused is described as follows: Perform routine stem cell isolation processes by using automated cell processing system Support execution of labbased Process Development activities and experiments Prepare related med المزيد...

Job DescriptionPosition Summary:Vertex Cell and Genetic Therapies (VCGT) is seeking a Senior Scientific Associate to join our dynamic Process Development Engineering Team in Boston MA. Cell and genetic therapies represent two rapidly emerging therapeutic modalities with the potential المزيد...

Job DescriptionVertex Pharmaceuticals is seeking a Research Scientist to join the Analytical Development Cell and Gene Therapy group. This position is expected to serve as a key contributor in expanding our capabilities for supporting drug substance and drug product program developmen المزيد...

Job DescriptionGeneral Summary:The Molecular Cell and Biology Research Scientist works with a some independence and is adept at conceptually outlining studies to design and execute focused research projects or a series of complex experimental procedures. These may include studying dis المزيد...