6149 - Senior CQV Engineer / Senior Validation Engineer 2
Verista, Inc.(11 days ago)
About this role
Verista is a life sciences consultancy that partners with pharmaceutical and biotech organizations to deliver commissioning, qualification, and validation services. The CQV Engineer role is a technical position within project teams working on regulated manufacturing and equipment implementation in FDA-regulated environments.
Required Skills
- Commissioning
- Qualification
- Validation
- GMP
- Change Management
- Root Cause Analysis
- Document Control
- Software Verification
- PLC Testing
- P&ID Review
+2 more
Qualifications
- Bachelor of Science in Technical Field (Engineering or Life Science)
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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