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Qa Validation Specialist Jobs (NOW HIRING)

LeadStack Inc.

GMP QA Validation Specialist

Durham, NC · On-site

$45 - $53/hr

QA Validation Specialist Location: Research Triangle Park, NC - 27709 Duration: 10 Months Pay Rate: $45/hr - $53/hr on W2 The Validations Contractor - GMP Quality Assurance, reporting to the ...

LeadStack Inc.

GMP QA Validation Specialist

Durham, NC · On-site

$45 - $53/hr

QA Validation Specialist Location: Research Triangle Park, NC - 27709 Duration: 10 Months Pay Rate: $45/hr - $53/hr on W2 The Validations Contractor - GMP Quality Assurance, reporting to the ...

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How much do qa validation specialist jobs pay per hour?

As of Aug 24, 2026, the average hourly pay for qa validation specialist in the United States is $50.45, according to ZipRecruiter salary data. Most workers in this role earn between $39.66 and $61.30 per hour, depending on experience, location, and employer.

What is a QA Validation Specialist?

QA Validation Specialists are professionals responsible for ensuring that processes, equipment, and systems in industries such as pharmaceuticals, biotechnology, and manufacturing meet established quality and regulatory standards. They design, execute, and document validation protocols to verify that all procedures and products comply with industry regulations and company requirements. Their work helps maintain product safety, efficacy, and compliance with agencies such as the FDA. QA Validation Specialists collaborate closely with quality assurance, production, and engineering teams to resolve issues and improve processes. This role often requires strong analytical skills, attention to detail, and knowledge of regulatory guidelines.

How does a QA Validation Specialist typically collaborate with other departments during the product development lifecycle?

QA Validation Specialists work closely with cross-functional teams, including R&D, manufacturing, and regulatory affairs, to ensure that products meet all quality and compliance standards before release. They participate in meetings to understand design specifications, develop validation protocols, and communicate test results. Effective collaboration is crucial for identifying potential issues early and implementing corrective actions, which helps streamline the validation process and ensures successful project outcomes. Regular interaction with other departments also provides valuable insight into the entire product lifecycle, enhancing both technical knowledge and teamwork skills.

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

To thrive as a QA Validation Specialist, you need a solid background in quality assurance, validation protocols, and regulatory compliance, often supported by a degree in life sciences or engineering. Familiarity with validation software, documentation management systems, and regulatory standards such as GMP and FDA guidelines is typically required. Attention to detail, analytical thinking, and strong communication skills set top performers apart in this role. These skills ensure that products and processes consistently meet quality standards and regulatory requirements, minimizing risks and ensuring compliance.

What is the difference between Qa Validation Specialist vs Quality Assurance Analyst?

AspectQa Validation SpecialistQuality Assurance Analyst
CertificationsGxP, ISO, or industry-specific validation certificationsISO, Six Sigma, or general QA certifications
Work EnvironmentRegulated industries like pharmaceuticals, biotech, medical devicesVarious industries including manufacturing, software, healthcare
Employer UsageCompanies requiring validation of systems/equipmentOrganizations focusing on process and product quality

Qa Validation Specialists focus on validating systems and equipment to meet regulatory standards, primarily in regulated industries. Quality Assurance Analysts oversee overall quality processes, often across diverse sectors. While both roles ensure quality, the Validation Specialist emphasizes compliance and validation protocols, whereas the Analyst concentrates on process improvement and defect prevention.

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Qa Validation Specialist jobs near you
Infographic showing various Qa Validation Specialist job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 12% Part Time, and 2% Contract. Highlights an 79% Physical, 2% Hybrid, and 19% Remote job distribution, with an average salary of $104,945 per year, or $50.5 per hour.

Quality Assurance Validation Specialist

Eliquent Life Sciences, Inc

Columbus, OH • On-site

$100K/yr

Full-time, Part-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 3 days ago

New

Job description

ELIQUENT Life Sciences is the leading global consulting firm providing solutions to life science companies researching, developing, and manufacturing innovative products to serve patients and respond to public health challenges around the world. ELIQUENT is committed to serving clients’ needs with extensive expertise, unwavering integrity, and strategic insight in a manner that supports availability of safe, effective, and high-quality drugs, biologics, and medical devices. For more information, please visit our website at eliquent.com.


We at Eliquent are looking for an experienced QA Validation Specialist to immediately join our consulting team onsite in Columbus, OH. The QA Validation Specialist will be responsible for:

  • On-site review of IQ/OQ/PQ protocols for the installation of new equipment and product lines
  • Reviewing and assessing validation impact for various activities
  • Participating in risk assessments to ensure compliance with GMP and validation requirements
  • Ensuring validated systems remain compliant through periodic reviews and lifecycle management.


Qualifications / Experience:

  • 3 to 7 years of experience in Quality Assurance, Validation, Quality Systems, or a related role within a regulated industry.
  • Experience supporting validation lifecycle activities, including qualification, protocol execution, reporting, and change management.
  • Working knowledge of cGMP, GxP, FDA, EMA, ISO, or other applicable regulatory requirements.
  • Experience authoring, reviewing, and executing validation documentation, including IQ/OQ/PQ protocols and reports.
  • Knowledge of process validation, equipment qualification, and/or cleaning validation.
  • Familiarity with change control, CAPA, deviation investigations, and risk assessments.
  • Strong technical writing and documentation skills.
  • Experience with electronic Quality Management Systems (eQMS), document management systems, and Microsoft Office Suite. Understanding of data integrity requirements and validation lifecycle principles.
  • Education: Bachelor's degree in Engineering, Life Sciences, Biology, Chemistry, Quality Assurance, Computer Science, or a related technical field



What We Offer:

  • Competitive Compensation: Attractive salary and comprehensive benefits package for full-time and part-time employees, including health, dental, vision, and life insurance, a 401(k) plan with employer match, a generous paid time off policy, and additional perks. Compensation is commensurate with professional experience.
  • Career Development: Opportunities for professional growth and advancement within a supportive and innovative environment.
  • Work-Life Balance: Flexible work arrangements and a commitment to maintaining a healthy work-life balance.

Eliquent Life Sciences is proud to be an Equal Opportunity Employer, committed to employee diversity.