Lab CSV Engineer​/Senior CSV Engineer

Description 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 solve some of the world’s most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities.

Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day.

• 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.
• We constantly acquire new skills and learn from our experiences to enhance our collective expertise

• Lead and execute computer system validation and equipment qualification activities for laboratory equipment integrated with Lab Vantage LIMS in a GxP-regulated environment
• Qualify and validate laboratory instruments and systems, with a primary focus on Climet environmental monitoring instruments and similar laboratory equipment that interface with Lab Vantage
• Execute vendor-provided qualification documentation and protocols, including SAT, IQ, OQ, and related testing, ensuring activities are performed in accordance with approved procedures and protocols
• Support the execution and documentation of qualification activities for laboratory instruments, primarily using existing approved protocols and documentation with minor updates to reflect equipment-specific differences
• Leverage existing approved validation and qualification documentation to efficiently develop or update URS, risk assessments, IQ/OQ documentation, test scripts, traceability, and validation summary documentation for equipment that is substantially equivalent to existing qualified units
• Evaluate existing equipment qualification and validation packages to identify required updates based on instrument configuration, LIMS integration, software, hardware, or other equipment-specific differences
• Perform and document testing of LIMS interfaces and data flows associated with laboratory instruments, ensuring accurate, complete, and reliable transfer of data between equipment and Lab Vantage
• Review vendor documentation and protocols for completeness and applicability and identify any gaps or deviations requiring resolution prior to or during execution
• Execute validation and qualification activities in accordance with GxP, data integrity, 21 CFR Part 11, company validation procedures, and applicable CSV/CSA principles
• Document test results, deviations, discrepancies, and exceptions and support resolution through appropriate investigation, change control, and CAPA processes
• Collaborate with Laboratory, Quality, IT, Validation, equipment vendors, and system owners to coordinate qualification activities and resolve technical or documentation issues
• Support validation documentation closeout, ensuring qualification packages are complete, accurate, traceable, and audit-ready
• Provide technical support for the laboratory equipment and Lab Vantage environment following qualification, including troubleshooting and assessment of changes impacting the validated state

• Bachelor’s degree in Engineering, Computer Science, Life Sciences, Information Systems, or related technical discipline
• 5+ years of CSV, equipment qualification, or validation experience in a regulated life sciences environment
• 2–3+ years of experience qualifying laboratory equipment integrated with a LIMS, with hands‑on Lab Vantage LIMS experience strongly preferred
• Demonstrated experience executing vendor-provided qualification protocols, including SAT and IQ/OQ, and accurately documenting test results, deviations, and exceptions
• Experie…