Verista, Inc.

6111 - CQV Engineer / Validation Engineer

Verista, Inc.

2 months ago
Thousand Oaks, CA
Onsite
Full Time
Medior
0 applicants
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Verista, Inc.
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About this role

The Validation Engineer will support the successful startup and qualification of a new early-phase clinical manufacturing facility, working within a regulated life sciences environment. The role involves ensuring activities meet regulatory and cGMP expectations, supporting audit readiness, and contributing to the organization’s mission to enable life sciences clients to improve lives. The position is part of a collaborative, team-oriented culture focused on quality and compliance.

Skills

Qualifications

Bachelor's Degree in Engineering, Life Sciences, or Related Field
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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