5910 - CSV Engineer / Validation Engineer
Verista, Inc.(13 days ago)
About this role
A Validation Engineer at Verista is a technical consultant within the company’s life-sciences practice, supporting clients in pharmaceutical and biotech industries. The role contributes to maintaining inspection-ready validated computerized systems and helps ensure regulatory compliance as part of Verista’s broader consulting services.
Required Skills
- Computer Validation
- Electronic Batch
- MES
- cGMP
- GAMP 5
- IQ/OQ/PQ
- Risk Assessment
- URS/FDS
- Deviation Management
- Change Control
+4 more
Qualifications
- Bachelor's Degree in Engineering, Computer Science, or Life Sciences
About Verista, Inc.
verista.comVerista is a life‑sciences consulting and engineering firm that supports pharmaceutical, biotech, medical device, and consumer‑health companies across the entire product lifecycle. They specialize in validation, quality and regulatory compliance, engineering and automation, commissioning/qualification, computer system validation, and digital transformation. Verista combines domain‑specific technical expertise and regulatory know‑how with hands‑on implementation to reduce risk, accelerate timelines, and ensure GxP compliance for complex manufacturing, clinical, and commercial operations.
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