6119 - CQV Engineer / Senior Validation Engineer
Verista, Inc.(25 days ago)
About this role
Verista is hiring a mid-to-senior Validation Engineer to support CapEx and OpEx projects at a pharmaceutical manufacturing facility, focusing on automation commissioning and qualification of process equipment. The role involves ensuring compliance with cGMP and regulatory standards, supporting facility commissioning milestones, and collaborating with Engineering, QA, Operations, and Automation teams. The position is onsite in Norton, MA and may require occasional after-hours support for validation activities.
Required Skills
- Commissioning
- Qualification
- Documentation
- Project Planning
- Collaboration
- Testing
- Troubleshooting
- Automation
- Thermal Mapping
- Cleaning Validation
+2 more
Qualifications
- Bachelor's Degree (STEM Preferred)
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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