Search the 28 jobs at Verista

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

The Senior Automation Engineer will provide coordination and integrated automation support for robotics asset portfolios, focusing on delivery and troubleshooting within pharmaceutical environments. Responsibilities include system troubleshooting, Factory Acceptance Testing, production evaluation, documenting changes, and team contributions for project completion.

As a Senior Automation Engineer, you will coordinate Automation Support within the Global Robotics Asset Portfolio, ensuring the delivery of automated applications for pharmaceutical environments. Responsibilities include troubleshooting, conducting Factory Acceptance Testing, optimizing production metrics, and managing documentation. Travel to multiple client sites is required.

As a Senior CSV Engineer/Analyst at Verista, you will provide IT CSV support for implementing and validating electronic systems, collaborate with stakeholders on project tracking, review documentation for compliance, and engage in quality improvement initiatives. You’ll also manage project timelines and assist in change controls for computer systems.

The Lead CSV Engineer/Analyst at Verista is responsible for authoring and executing technical documentation for system validation, conducting user interface testing, and collaborating with engineering teams to ensure compliance with industry standards. The role involves risk assessments and modifications based on testing results.

The Senior Project Manager will oversee project tasks and teams, ensuring that client demands and project scope, budget, and timelines are met. Responsibilities include materials planning, cost control, project scheduling, managing resources, and facilitating communication among cross-functional teams. The role involves problem-solving, risk management, and regular project reporting to stakeholders.

The Lead CQV Engineer/Analyst is responsible for authoring and executing commissioning, qualification, and validation documentation, running tests, and ensuring compliance with regulatory standards in pharmaceutical or biotech environments. This role includes leading CQV efforts in facilities and utilities, developing validation protocols, and conducting risk assessments while collaborating with engineering teams.