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Capa Validation Engineer Jobs (NOW HIRING)

Pinnaql

Validation Engineer

Wilson, NC · On-site

Support deviations, investigations, CAPA, and change control activities associated with validation projects. * Review engineering and technical documentation to ensure validation requirements are ...

Pinnaql

Validation Engineer

Wilson, NC · On-site

Support deviations, investigations, CAPA, and change control activities associated with validation projects. * Review engineering and technical documentation to ensure validation requirements are ...

Agilent

Validation Engineer

Boulder, CO · On-site

Resolve CAPA's, nonconformances, protocol incidents, and change controls related to validation ... S.) or equivalent in engineering or life sciences fie * 1+ years relevant experience. * Should ...

Agilent

Validation Engineer

Frederick, CO · On-site

Resolve CAPA's, nonconformances, protocol incidents, and change controls related to validation ... S.) or equivalent in engineering or life sciences fie * 1+ years relevant experience. * Should ...

Agilent

Validation Engineer

Frederick, CO · On-site

Resolve CAPA's, nonconformances, protocol incidents, and change controls related to validation ... S.) or equivalent in engineering or life sciences fie * 1+ years relevant experience. * Should ...

Mativ

Validation Engineer

Dallas, TX · On-site

Validation Engineer Mativ is a global leader in specialty materials headquartered in Alpharetta ... Resolve CAPA's, non-conformances, protocol incidents, and change controls related to validation ...

System One

Validation Engineer

Athens, GA · On-site

$45 - $48/hr

Aseptic Manufacturing Validation Engineer Location: Athens, GA Type: 12 month contract Compensation ... Experience with validation documentation, CAPA investigations, change control processes, and ...

System One Holdings, LLC

Validation Engineer

Athens, GA · On-site

$45 - $48/hr

Aseptic Manufacturing Validation Engineer Location: Athens, GA Type: 12 month contract Compensation ... Experience with validation documentation, CAPA investigations, change control processes, and ...

System One

Validation Engineer

Athens, GA · On-site

$45 - $48/hr

Aseptic Manufacturing Validation Engineer Location: Athens, GA Type: 12 month contract Compensation ... Experience with validation documentation, CAPA investigations, change control processes, and ...

System One

Validation Engineer

Athens, GA · On-site

$45 - $48/hr

Aseptic Manufacturing Validation Engineer Location: Athens, GA Type: 12 month contract Compensation ... Experience with validation documentation, CAPA investigations, change control processes, and ...

System One

Validation Engineer

Athens, GA · On-site

$45 - $48/hr

Aseptic Manufacturing Validation Engineer Location: Athens, GA Type: 12 month contract Compensation ... Experience with validation documentation, CAPA investigations, change control processes, and ...

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Capa Validation Engineer information

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How much do capa validation engineer jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for capa validation engineer in the United States is $52.00, according to ZipRecruiter salary data. Most workers in this role earn between $39.42 and $63.22 per hour, depending on experience, location, and employer.

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Infographic showing various Capa Validation Engineer job openings in the United States as of August 2026, with employment types broken down into 94% Full Time, 2% Part Time, and 4% Contract. Highlights an 85% Physical, 5% Hybrid, and 10% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

Validation Engineer

Wilson, NC • On-site

Pinnaql
Pharmaceutical and Medicine Manufacturing • 11 - 50 employees
Learn more about Pinnaqlexternal

Full-time

Posted 28 days ago

Job description

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:
  • Validation Engineer

Position Overview
We are seeking an experienced Validation Engineer with Commissioning, Qualification & Validation (CQV) experience to support projects within the life sciences industry. The successful candidate will be responsible for executing and documenting commissioning, qualification, and validation activities for facilities, utilities, equipment, systems, and manufacturing processes in accordance with applicable regulatory requirements and Good Manufacturing Practices (GMP).
This role requires strong technical documentation skills, attention to detail, and the ability to work collaboratively with Engineering, Quality, Manufacturing, Automation, and Project Management teams.
Key Responsibilities
  • Execute and support Commissioning, Qualification & Validation (CQV) activities for pharmaceutical, biotechnology, medical device, or other regulated life sciences facilities.
  • Develop, review, and execute validation documentation, including:
    • Validation Plans
    • User Requirements Specifications (URS)
    • Risk Assessments
    • Design/Functional Specifications
    • Commissioning documentation
    • IQ/OQ/PQ protocols and reports
    • Traceability Matrices
    • Summary Reports
  • Support qualification of equipment, facilities, utilities, and manufacturing systems.
  • Perform protocol execution, field verification, data collection, and review of qualification results.
  • Ensure validation activities are performed in compliance with GMP, FDA, EU GMP, and applicable industry standards.
  • Participate in FMEA/risk assessments and apply a risk-based approach to validation activities.
  • Support deviations, investigations, CAPA, and change control activities associated with validation projects.
  • Review engineering and technical documentation to ensure validation requirements are adequately addressed.
  • Collaborate with Engineering, Quality Assurance, Manufacturing, Automation, Facilities, and other project stakeholders.
  • Track validation deliverables, schedules, open items, and project milestones.
  • Support commissioning activities and transition from commissioning into formal qualification.
  • Ensure validation documentation is complete, accurate, and audit-ready.
  • Participate in client meetings, project status meetings, and technical reviews.
  • Provide technical support during regulatory or client inspections, as required.

CQV Experience
Candidates should have hands-on experience with some combination of:
  • Commissioning and qualification of process equipment
  • Facility and utility qualification
  • Cleanrooms and controlled environments
  • HVAC systems
  • Purified Water / WFI systems
  • Compressed gases and process gases
  • Autoclaves, sterilizers, and/or depyrogenation equipment
  • Manufacturing and laboratory equipment
  • Temperature-controlled systems
  • Process systems and supporting utilities
  • Equipment and system turnover documentation
  • IQ/OQ/PQ execution

Required Qualifications
  • Bachelor's degree in Engineering, Science, or a related technical discipline.
  • 3+ years of validation, qualification, commissioning, or CQV experience within a regulated life sciences environment.
  • Experience working in pharmaceutical, biotechnology, medical device, or other GMP-regulated industries.
  • Strong understanding of GMP and validation principles.
  • Experience developing and/or executing validation and qualification protocols.
  • Experience with risk-based validation methodologies.
  • Strong technical writing and documentation skills.
  • Ability to interpret engineering drawings, specifications, procedures, and technical documentation.
  • Strong organizational and project management skills.
  • Ability to work independently and collaboratively in a project environment.

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.
Excited to build something meaningful together? We look forward to hearing from you.
Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.

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