6153 - Lead CQV Engineer/ Lead Validation Engineer
Verista, Inc.(1 day ago)
About this role
Verista is hiring a Lead Validation Engineer to manage GMP equipment installation, commissioning, and qualification projects for large-molecule biologics manufacturing. The role supports upstream and downstream bioprocessing systems and associated utilities, ensuring projects are executed safely, on schedule, and in compliance with regulatory and quality requirements.
Required Skills
- CQV
- CGMP
- Commissioning
- Qualification
- Validation
- IQ/OQ/PQ
- FAT/SAT
- Project Management
- Vendor Management
- Regulatory Compliance
+2 more
Qualifications
- Bachelor's Degree in Engineering or Life Sciences
- CQV
- PMP
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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