Verista Jobs in United States

+ Build instruments consumable including critical reagents master data in LIMS system+ Work with site leaders to identify capture update all master data for each site within VCGT Cambridge LC1 VMC site for GxP operations+ Lead QC QA MFG departments in build revision review approv ...

Verista empodera el crecimiento y la innovación dentro de la comunidad científica ayudando a investigadores, organizaciones y empresas a resolver algunos de los desafíos más apremiantes relacionados con la salud. Nuestros expertos trabajan junto con las marcas más reconocidas del ...

Job summary · We are seeking talented professionals to join our team in the vibrant Raleigh/Durham, NC area.As a Quality Assurance Specialist at Verista you will oversee compliance with cGMP and other regulatory standards for facilities equipment processes and documentation manag ...

We are seeking an experienced Master Planner & Buyer/Project Manager to join our team at Verista in Southington, CT. As a key member of our operations team you will be responsible for developing and maintaining GMP-compliant master production schedules within an Oracle ERP/MRP en ...

We are seeking a Risk Management Engineer to support the IDM Risk Management Turbo AC team. · ...

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The Senior Digital System Specialist will be responsible for the creation and revision, as well as review and approval of LIMS master data within the LabVantage Laboratory Information Management System (LIMS) implemented at the Vertex Cell and Gene Therapy all sites (LC1, Cambrid ...

We are seeking a Project Engineer to support manufacturing and equipment modification activities within a regulated pharmaceutical environment. · This role will be responsible for coordinating and executing engineering projects related to equipment relocation, testing, and valida ...

Verista empowers growth and innovation within the scientific community. · The Master Planner & Buyer/Project Manager plays a critical role in solving business needs of life science industry clients. · Responsibilities: · Develop GMP-compliant master production schedules using Ora ...

Support the design, installation, startup and qualification of a biologics formulation fill and finish facility. · ...

The Business Development/Client Partner role is responsible for developing and maintaining solid business relations with key account decision makers to drive business within the account base. · Responsible for creating and directing strategy for large or growing accounts includin ...

Senior Digital System Specialist / Business Analyst · Verista's 500 experts team up with the world's most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific communit ...

Veristas 500 experts team up with the worlds most recognizable brands in the life science industry to solve their business needs. · ...

+Job Summary · A senior CQV engineer/validation engineer at Verista will support clients in downstream process & CQV activities. · +ResponsibilitiesDownstream process and CQV support (ex. Chromatography, Centrifugation) · ...

Lead end-to-end Life Sciences projects ensuring on-time on-budget delivery that meets client and regulatory requirements Develop and manage detailed project plans schedules budgets and resources to drive results and maximize ROI Act as primary point of contact for clients vendors ...

We are seeking a mid-to-senior level Validation Engineer to support both Opex and Capex projects in a pharmaceutical manufacturing facility. · The role requires experience with automation commissioning and qualification of process equipment, · including operation within a plant a ...

The Validation Engineer will play a critical role in the successful startup and qualification of a new early-phase clinical manufacturing facility.This position is responsible for generating and executing commissioning and qualification protocols and producing summary reports. · ...

We empower and support our colleagues. We commit to client success at every turn. We have the courage to do the right thing. We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged. · CQV Engineer Responsibilities (Typical)Upstream/downs ...

Verista's 500 experts team up with the world's most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies ...

We are seeking an experienced Computer System Assurance (CSA) Consultant to support GxP compliance activities across Pharmacovigilance (PV), Clinical, and Regulatory Affairs systems. · • Provide CSA / CSV subject matter expertise across PV, Clinical, and Regulatory Affairs platfo ...