Verista

HQ
Fishers, Indiana, USA
402 Total Employees
Year Founded: 2020

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Jobs at Verista

Search the 27 jobs at Verista

Recently posted jobs

Pharmaceutical
The Project Manager serves as the Scrum Master, facilitating Agile ceremonies, collaborating with stakeholders, addressing project risks, and documenting changes. The role demands strong skills in project management tools and methodologies, ensuring projects are completed within scope, budget, and timeline.
Pharmaceutical
The Automation Engineer will provide technical support in programming and troubleshooting automated equipment, managing commissioning and qualification processes, and supporting integration of site automation systems. The role requires collaboration with site engineering teams to facilitate knowledge sharing and enhance operational efficiencies.
Pharmaceutical
The Automation Engineer will manage document control, oversee commissioning and qualification efforts, and ensure automation systems comply with regulatory standards. They will collaborate with cross-functional teams and manage documentation related to the automation process, vendor management, and compliance with Good Documentation Practices.
Pharmaceutical
The Senior IT Project Manager will plan and execute medium to large-scale projects, manage their deliverables, schedules, and financials, and ensure alignment with best practices. Responsibilities include stakeholder communication, risk evaluation, and obstacle removal to drive project momentum, all while adapting to changing priorities in a hybrid work environment.
Pharmaceutical
The MES Process Engineer will support the MES Syncade system within manufacturing processes, optimize workflows, design experiments, manage CAPAs, draft technical reports, and guide junior team members. The role involves ensuring compliance and effective communication within teams and clients.
11 Days Ago
United States
Remote
Pharmaceutical
The Lead CQV Engineer is responsible for overseeing the post go-live hypercare of the Med Safety systems, ensuring its effective operation and support during the critical initial phase after launch.
Pharmaceutical
The Data Integration Engineer will design, develop, and implement data integration solutions to support client needs. Responsibilities include collaborating with stakeholders to translate requirements into technical specifications, performing data analysis, maintaining data models, ensuring data quality, and providing support for data integration issues.
Pharmaceutical
The Senior Project Manager will oversee the strategic implementation of technology-enabled capabilities in the life sciences sector, specifically managing projects related to Salesforce and Oracle ERP systems, collaborating with various stakeholders, and ensuring successful project delivery through established methodologies and governance frameworks.
Pharmaceutical
The Senior Process Engineer will meet with client stakeholders to develop and execute Process Validation protocols. Responsibilities include coordinating testing and data collection, overseeing qualification efforts, maintaining compliance records, providing technical guidance to team members, and ensuring adherence to regulatory requirements.
Pharmaceutical
The SAS Analytics Administrator is responsible for implementing and supporting technology and informatics systems within various laboratory and clinical operations. This role requires translating business problems into technology solutions and project management, with an emphasis on R&D Clinical applications. Effective communication and a strong understanding of regulatory frameworks are essential.
19 Days Ago
Columbus, OH, USA
Pharmaceutical
The CQV Engineer is responsible for authoring and executing qualification documentation, running test scripts, ensuring compliance with project schedules, and maintaining detailed records for validation processes. This role involves user interface testing, software verification, and making recommendations based on test results within a team setting.
20 Days Ago
Livermore, CA, USA
Pharmaceutical
The Project Manager will oversee the planning and execution of medium to large-sized projects in the finance domain, ensuring all deliverables are met within time and budget. Responsibilities include managing project teams, collaborating with cross-functional resources, providing status reports, and monitoring costs and risks.
Pharmaceutical
The Documentation Control Lead / Project Engineer will manage validation documentation, ensuring compliance with FDA and cGMP standards, perform quality reviews, and collaborate with engineering teams. Responsibilities include overseeing document control activities and providing documentation for audits and inspections.
20 Days Ago
New Brunswick, NJ, USA
Pharmaceutical
The Lead CQV Engineer/Analyst is responsible for authoring and executing technical documentation for commissioning and validation. They oversee equipment qualification, conduct risk assessments, collaborate with engineering teams, and ensure compliance with regulatory standards, focusing on facilities and utilities in a pharmaceutical environment.
20 Days Ago
Norwood, MA, USA
Pharmaceutical
The Senior Automation Engineer will support on-site resources, set up and troubleshoot various automation equipment such as MES systems, printers, scales, and barcode scanners, and manage project deliverables. The role includes overseeing system integrations, coordinating engineering design and support, and facilitating communication with management and project teams.
Pharmaceutical
The Automation Engineer will provide technical support for programming and troubleshooting automated equipment including vision systems and robotics, particularly in pharmaceutical manufacturing. Responsibilities include supporting the commissioning and qualification of systems, code management, technical documentation updates, and knowledge sharing for continuous improvement. A key focus will be on high-speed assembly and automated systems.
Pharmaceutical
The Automation Engineer will provide technical support for programming and automation of equipment, including vision systems and robotics, primarily for pharmaceutical manufacturing. Responsibilities include troubleshooting, overseeing commissioning and qualification testing, code management, and supporting site engineering initiatives.
Pharmaceutical
The Automation Engineer is responsible for the design and implementation of automation aspects in equipment projects, including PLC and HMI programming, ensuring compliance with quality standards and regulations, and managing change control. They will carry out testing, maintain documentation, and support clients in validation efforts while leading small project teams.
Pharmaceutical
The Project Manager is responsible for leading life science projects to meet client demands, managing project scope, budget, and timelines, and ensuring effective communication with stakeholders. They will develop detailed project plans, address technical issues, and collaborate with cross-functional teams to achieve project outcomes and monitor financial performance.
Pharmaceutical
The Principal Application Development Lead will oversee the design, implementation, and optimization of Clinical LIMS applications. Responsibilities include leading application development, ensuring system integration and data integrity, customizing solutions for client needs, ensuring regulatory compliance, and managing project timelines and deliverables.