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Validation Coordinator Jobs (NOW HIRING)

Herbalife

Engineer, Validation

Lake Forest, CA · On-site

The Validation Engineer is responsible for all equipment and process validation activities at ... Coordinates change control and equipment-related changes (this includes providing assessment and ...

Herbalife

Engineer, Validation

Lake Forest, CA

The Validation Engineer is responsible for all equipment and process validation activities at ... Coordinates change control and equipment-related changes (this includes providing assessment and ...

Herbalife

Engineer, Validation

Lake Forest, CA

The Validation Engineer is responsible for all equipment and process validation activities at ... Coordinates change control and equipment-related changes (this includes providing assessment and ...

Valspec

Validation Engineer

Upper Gwynedd, PA · On-site

Validation Engineer (Junior-Mid Level) Employment Type: W2 Contract (no C2C) Duration: Long-term ... Light project coordination or PM experience Contract Duration This W2 contract supports a multi ...

Fresenius Kabi

Manager Validation

Wilson, NC · On-site

Manages Coordination of qualification and re-qualification of manufacturing equipment. Review and approval of Protocols (Installation Qualification, Operational Qualification, Performance ...

Automated Systems, Inc.

Be Seen First

Validation Engineer

Chicago, IL · On-site

$45 - $65/hr

... coordination, issue resolution, and user training Education and Experience Requirements: · Bachelor's degree in Pharmacy, Engineering, or a related scientific discipline · 3+ years of validation ...

Freseniusglobal

Manager Validation

Wilson, NC · On-site

Manages Coordination of qualification and re-qualification of manufacturing equipment. Review and approval of Protocols (Installation Qualification, Operational Qualification, Performance ...

Fresenius Kabi USA, LLC

Validation Engineer

Wilson, NC

$60K - $85K/yr

... initial validation and equipment/system requalification's. Will participate in equipment ... Coordinates and communicates all testing with affected functional groups and evaluates test results.

Kelly Services

Validation Engineer

Charles City, IA

Coordinating equipment and facility qualification activities between Engineering, Maintenance, QA, Operations, construction firms, and validation contractors. Coordinating with Maintenance to repair ...

Cryoport

Validation Engineer

Irvine, CA · On-site

POSITION SUMMARY: The Validation Engineer - Consulting Services will support the Consulting ... Assists with coordination between external third-party testing laboratories to ensure protocol ...

Medline

Validation Engineer

Hartland, WI · On-site

$73K - $110K/yr

... coordination of computer and test method validations of applicable products. * Validate new and ... revalidate as appropriate existing equipment used in OTC/Cosmetic and medical device manufacturing.

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How much do validation coordinator jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for validation coordinator in the United States is $23.32, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $25.96 per hour, depending on experience, location, and employer.

What are some common challenges faced by Validation Coordinators when managing multiple projects simultaneously?

Validation Coordinators often juggle several projects at once, each with its own timeline, regulatory requirements, and stakeholders. A common challenge is prioritizing tasks effectively while ensuring that all validation documentation is accurate and compliant with industry standards. Coordinators must also communicate clearly with cross-functional teams, such as quality assurance, manufacturing, and engineering, to resolve issues quickly and keep projects on schedule. Developing strong organizational skills and adapting to shifting priorities are key to success in this role.

What is a Validation Coordinator?

A Validation Coordinator is a professional responsible for overseeing and managing the validation processes within industries like pharmaceuticals, biotechnology, or manufacturing. Their main role is to ensure that equipment, systems, and processes consistently produce results that meet quality and regulatory standards. They coordinate validation activities, maintain documentation, and collaborate with cross-functional teams to ensure compliance. Validation Coordinators play a key role in quality assurance by planning and executing validation protocols and handling audits or inspections.

What are the key skills and qualifications needed to thrive as a Validation Coordinator, and why are they important?

To thrive as a Validation Coordinator, you need a solid background in quality assurance, regulatory compliance, and process validation, often supported by a degree in life sciences or engineering. Familiarity with validation protocols, Good Manufacturing Practices (GMP), and systems like TrackWise or MasterControl is typically required. Attention to detail, strong organizational skills, and effective communication set standout candidates apart in this role. These skills ensure that processes and products consistently meet regulatory standards, minimizing risk and ensuring product quality.
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Validation Coordinator jobs near you
Infographic showing various Validation Coordinator job openings in the United States as of May 2026, with employment types broken down into 1% As Needed, 92% Full Time, 4% Part Time, 1% Temporary, and 2% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $48,503 per year, or $23.3 per hour.

Validation Engineer

Stark Pharma Solutions Inc

Fort Worth, TX • On-site

Contractor

Posted 28 days ago

Job description

Job Title: Validation Engineer

Location: Fort Worth, TX (Local candidates only)

Travel: Required – Alabama (3–4 weeks, expenses paid)

Duration: 3–6 Month Contract

Start Date: Immediate

Job Summary

We are seeking a Validation Engineer to support EO sterilization validation activities within a regulated manufacturing environment. This role will focus on supervising and coordinating Performance Qualification (PQ) execution activities while ensuring compliance with GMP and ALCOA+ documentation standards.

The ideal candidate will have hands-on experience with sterilization validation processes, strong coordination skills, and the ability to support cross-functional execution activities in a fast-paced environment.

Key Responsibilities

  • Supervise execution of EO sterilization Performance Qualification (PQ) activities
  • Coordinate half-cycle, nominal/full-cycle, and maximum-cycle sterilization runs
  • Prepare and manage PCDs (Process Challenge Devices) and Biological Indicators (BIs) for shipment and cycle insertion
  • Support preparation and arrangement of dunnage for EO sterilization processes
  • Oversee movement of product loads through refrigerated storage, tempering, sterilization, and aeration processes
  • Coordinate retrieval and shipment of PCDs, BIs, and product samples for Quality Control testing
  • Ensure execution activities and documentation comply with ALCOA+ principles and GMP requirements
  • Collaborate with Validation, Quality, and Operations teams to support project timelines and execution

Required Qualifications

  • Experience in validation within medical device, pharmaceutical, or regulated manufacturing environments
  • Hands-on knowledge of EO sterilization validation and PQ execution activities
  • Strong understanding of GMP documentation practices and ALCOA+ principles
  • Ability to coordinate cross-functional activities and manage execution timelines
  • Strong communication and organizational skills