6111 - CQV Engineer / Validation Engineer

Verista, Inc.(26 days ago)

Thousand Oaks, CAOnsiteFull TimeMedior$65,000 - $86,276Validation

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.

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Required Skills

Commissioning
Qualification
Validation
Documentation
Data Collection
Problem Solving
Cross-Functional Collaboration
Deviations Management
cGMP
Regulatory Knowledge

+5 more

Qualifications

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

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.