Search the 24 jobs at Verista

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 Staff Analyst collaborates with clients and team members on various projects, focusing on tasks such as system testing, document creation for Quality Management Systems, and data analysis. Responsibilities include drafting and executing test scripts, preparing test plans, and resolving system issues.

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 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.

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.

The Field Automation Engineer will be responsible for configuring and testing automated equipment, setting up vision systems, installing equipment at client locations, and troubleshooting automation challenges. The role requires both remote and onsite support and involves managing multiple projects while collaborating with automation engineers.

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 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 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.

The Senior Quality Specialist will oversee quality processes for Cell and Gene Therapy operations, including batch disposition, quality investigations, and compliance with GMP regulations. Responsibilities include leading quality assurance efforts for manufacturing operations, reviewing documentation, providing training, and supporting change controls and CAPAs.

Process Engineers are responsible for supporting design, scale-up, product development, and operational improvements in pharmaceutical manufacturing environments. They investigate manufacturing processes, design and execute experiments, and write technical reports for process changes and regulatory filings. This is an entry-level position suitable for recent college graduates.

The Scrum Master will lead multiple Scrum teams in a transformation program, facilitating Agile delivery and managing product backlogs. The role includes coaching a junior Scrum Master and working closely with Product Owners to gather customer feedback. Experience in a regulated biopharma environment is essential, alongside strong communication skills.

The Automation Engineer will program and troubleshoot automated equipment like vision systems and Fanuc robotics, offering support during the equipment commissioning and qualification phases. They will assist site engineering initiatives, perform source code management, and ensure proper technical documentation and continuous improvement communication.

The Automation Engineer will manage the lifecycle of project-related documents for automation and commissioning, ensuring compliance with regulatory standards. Responsibilities include developing commissioning schedules, managing vendor interactions, conducting Factory and Site Acceptance Testing, and ensuring documentation aligns with Good Documentation Practices for audit readiness.

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 Senior Quality/GxP Auditor is responsible for developing compliance plans, consulting clients on best practices, mentoring team members, supporting audits, ensuring client compliance with regulations, and identifying areas for business expansion. The role requires strong communication skills and expert knowledge of GxP requirements.