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Validation Coordinator Jobs (NOW HIRING)

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 ...

Ensuring the timely development, execution, and coordination of all validation activities pertaining to facility, equipment, and process in compliance with Quality System requirements, 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 ...

Validation Engineer

Caguas, PR · On-site

$85 - $115/hr

Hands-on role focused on protocol execution, technical troubleshooting, and direct coordination ... Support the full Validation Life Cycle: planning, URS/FRS, risk assessment (FMEA), RTM, execution ...

Strong technical writing, documentation, organizational, and project coordination skills. * Ability to work collaboratively with cross-functional teams and manage multiple validation activities ...

Validation Specialist

Aibonito, PR · On-site

$85 - $120/hr

Strong technical writing, documentation, organizational, and project coordination skills. * Ability to work collaboratively with cross‑functional teams and manage multiple validation activities ...

New

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

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.

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.

Strong project coordination skills, including planning, prioritizing, and tracking validation activities. * Effective stakeholder management skills with the ability to collaborate across Quality ...

New

Validation Engineer What you will do Let's do this. Let's change the world. In this vital role is ... Strong verbal communication and project coordination skills, with the ability to work effectively ...

New

$86 - $116/hr

Validation EngineerWhat you will do Let's do this. Let's change the world. In this vital role is ... Strong verbal communication and project coordination skills, with the ability to work effectively ...

Posted today

... 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.

Validation Engineer

Lakewood, NJ · On-site

$77K - $95K/yr

Review and resolve validation questions, deviations, and errors in coordination with departmental managers * Maintain accurate, FDA-compliant documentation of all validation studies and reports

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.

Showing results 41-60

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How much do validation coordinator jobs pay per hour?

As of Aug 21, 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 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?

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.

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.
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Infographic showing various Validation Coordinator job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 75% In-person, and 25% Hybrid job distribution, with an average salary of $48,503 per year, or $23.3 per hour.

Engineer, Validation

Herbalife

Lake Forest, CA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 23 days ago


Job description

Join an award-winning team at one of Orange County's Top Workplaces! Herbalife at Lake Forest has been recognized by the OC Register for our exceptional workplace culture, and we're looking for a dedicated Engineer, Validation to help us maintain our world-class standards.

ROLE AT A GLANCE: 

This is your opportunity to play a critical role in ensuring the products that improve millions of lives around the world are manufactured with the highest level of quality, safety, and integrity.

The Validation Engineer is responsible for all equipment and process validation activities at Herbalife Innovation and Manufacturing site, with primary focus at the Lake Forest location. Execution of validation activities is done to state and federal regulatory requirements, Herbalife and/or other applicable regulations and standards. The Validation Engineer supports all projects required for the expansion and improvement of operations at the production facility and coordinates all validation activities and projects with departmental managers.

The person in this role will be working around ingredients such as powder, milk, soy, & gluten.

In this role, you will be empowered to take ownership, drive meaningful improvements, and be recognized as a trusted technical authority across the organization

HOW YOU’LL MAKE AN IMPACT: 

Every validation you complete helps ensure that a product meeting the highest quality standards reaches someone who depends on it. Here's how you'll do that day to day:

  • Facilitates validation/qualification projects (planning, scheduling, execution, project reports, etc.).
  • Creates validation protocols and summary reports in compliance with Herbalife standards and/or government regulations. This includes investigating and resolving protocol deviations in a timely manner.
  • Coordinates change control and equipment-related changes (this includes providing assessment and feedback regarding change requests for equipment, facility, process modifications, etc.).
  • Maintains SOPs related to validation/qualification (i.e. validation master plans, validation templates) and update them, as required, to meet current standards.
  • Acts as back-up for management of the Global Environmental Monitoring (EM) program, which includes acting as an administrator for the associated Vaisala viewLinc application and working with temperature & humidity data loggers.
  • Additional duties as assigned.

TEAM DYNAMICS:  

You'll be joining a collaborative, passionate team that values expertise, mutual respect, and a shared drive to get it right. Your voice matters here — your insights and technical recommendations will directly shape how we operate.

  • Be able to work effectively with interdisciplinary departments to meet project deadlines and serve as a validation authority consulting with Engineering, Operations, and Quality.

LEADERSHIP AND SUPERVISORY RESPONSIBILITIES: 

Not applicable for this position.

Your technical expertise directly supports the team who help make our amazing products.


Experience

We're looking for someone who brings real-world GMP expertise and is ready to make an immediate impact:

  • 3-5 years of validation/qualification and process engineering experience in a GMP environment.
  • 5+ years of experience in Good Manufacturing Practices and Good Documentation Practices.
  • Experience in food, pharmaceutical and/or medical device process development.

QUALIFICATIONS FOR SUCCESS: 

Education

  • Bachelor of Science in Chemistry or field of Engineering 

Skills/Certifications 

  • Strong technical writing skills. Detailed knowledge of grammar, spelling, punctuation, and the fundamentals of technical GMP documentation.
  • Strong mechanical aptitude and process knowledge. Ability to work independently with minimal supervision.
  • Knowledge of PLC and automated controls qualification.
  • Knowledge of qualification fundamentals and requirements for powder and liquid handling, processing, and packaging.
  • Basic experience with equipment cleaning and computer systems validation methodologies is a plus.
  • Experience in electronic validation systems is preferred but not required.
  • Openness to learning skills outside of validation but is required for the expansion and improvement of operations at the production facility.

Ready to bring your validation expertise to a company with real global impact? Apply today and become part of the Herbalife team.

#LI-NP1


Herbalife offers a variety of benefits to eligible employees in the U.S. (limited to the 50 States and the District of Columbia), which includes Group Health Programs, other Voluntary Benefit Programs, and Paid Time Off. Group Health Programs include Medical, Dental, Vision, Health Savings Account (HSA), Flexible Spending Accounts (FSA), Basic Life/AD&D; Short-Term and Long-Term Disability, and an Employee Assistance Program (EAP). Other Voluntary Benefit Programs include a 401(k) plan, Wellness Incentive Program, Employee Stock Purchase Plan (ESPP), Supplemental Life/Critical Illness/Hospitalization/Accident Insurance, and Pet Insurance. Paid time off includes Company-observed U.S. Holidays, Floating Holidays, Vacation, Sick Time, a Volunteer Program, Paid Maternity and Paternity Leave, Bereavement Leave, Personal Leave and time off for voting.