Verista, Inc.

6242 - Upstream Principal CQV Engineer / Lead Validation Engineer

Verista, Inc.

3 days ago
Holly Springs, NC
Onsite
Full Time
Senior
0 applicants
Verista, Inc.
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About this role

Verista is seeking a CQV Engineer with experience in upstream bioprocessing systems to support commissioning, qualification, and validation activities in biopharmaceutical manufacturing. The role involves working cross-functionally to ensure systems meet quality and regulatory standards, with a focus on upstream operations and process equipment.

Skills

Verista, Inc.

About Verista, Inc.

verista.com

Verista 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.

About Verista, Inc.

Headquarters

San Francisco, CA

Company Size

201-500 employees

Founded

2018

Industry

Technology

Glassdoor Rating

4.2 / 5

Leadership Team

Sarah Johnson

Chief Executive Officer

Michael Chen

Chief Technology Officer

Emily Williams

VP of Engineering

David Rodriguez

VP of Product

Jessica Thompson

Chief Financial Officer

Andrew Park

VP of Sales

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