Valspec
Valspec6d ago
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CQV Consultant

Non Headquartersmid
OtherConsultant
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Quick Summary

Overview

Valspec—a global provider of system validation and lifecycle services—provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. Established in 1999,

Technical Tools
OtherConsultant

Valspec—a global provider of system validation and lifecycle services—provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. Established in 1999, Valspec’s mission is to provide a wide spectrum of services that help its clients meet their capital project and lifecycle maintenance goals.

Valspec’s projects are critical to the industry, and to the people who rely on its products. Many projects ensure that life-changing drugs are available to those who need them; others streamline production to meet demand at a lower cost, allowing for the discovery of new and innovative therapies.

Requirements

~1 min read

We are hiring CQV professionals with experience in one or more of the following areas:

  • Upstream Processing
  • Downstream Processing
  • CIP (Clean-in-Place) Systems
  • PSE (Process Support Equipment)
  • Clean Utilities
  • Prior CQV experience in pharmaceutical, biotech, or GMP-regulated manufacturing environments
  • Strong knowledge of commissioning and qualification processes
  • Experience supporting one or more of the following: Upstream, Downstream, CIP, PSE, or Clean Utilities systems
  • Familiarity with GMP documentation practices and regulatory requirements
  • Ability to work onsite in Holly Springs, NC on a full-time basis
  • Strong communication and cross-functional collaboration skills

Responsibilities

~1 min read
  • Execute CQV lifecycle activities including commissioning, IQ/OQ, and field verification
  • Support startup and qualification of GMP manufacturing equipment and utility systems
  • Author, review, and execute validation documentation and protocols
  • Coordinate with engineering, operations, quality, automation, and project teams
  • Support deviation investigations, change controls, and CAPA activities
  • Ensure compliance with GMP, FDA, and regulatory requirements
  • Participate in walkdowns, system turnover, and punch-list resolution
  • Maintain accurate documentation in accordance with data integrity and quality standards

Nice to Have

~1 min read
  • Large-scale biologics or vaccine manufacturing projects
  • Startup or greenfield facility experience
  • Experience with DeltaV, MES, or automated process systems
  • Knowledge of clean utilities including WFI, clean steam, compressed gases, and purified water systems

 

What We Offer

~2 min read

At Valspec, we offer more than just a job — we provide a career experience rooted in a standout culture, collaborative environment, and a strong sense of ownership. As an Employee Stock Ownership Plan (ESOP) company, every team member has a stake in our success, fostering a shared commitment to excellence and innovation.  We also offer a highly competitive benefits package, including:

Premium medical coverage
401(k) with company match
Tuition reimbursement
Unique performance incentives
And more — all designed to support your growth, well-being, and future.

Location & Eligibility

Where is the job
Non Headquarters
On-site at the office
Who can apply
Same as job location

Listing Details

Posted
May 19, 2026
First seen
May 21, 2026
Last seen
May 26, 2026

Posting Health

Days active
0
Repost count
0
Trust Level
60%
Scored at
May 21, 2026

Signal breakdown

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Valspec
Valspec
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Employees
125
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ValspecCQV Consultant