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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.
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