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Equipment Qualification Validation Engineer Jobs

Validation Engineer

Athens, GA Β· On-site

$45 - $48/hr

Aseptic Manufacturing Validation Engineer Location: Athens, GA Type: 12 month contract Compensation ... equipment, utilities, and facilities. This role is responsible for qualification, protocol ...

CQV Engineer

Indianapolis, IN Β· On-site

$80K - $95K/yr

The Validation Engineer is an FTE project based role.β€―The Validation Engineer is responsible for ... validation documents for new cleanrooms and packaging equipment, including utilities qualification ...

Validation Engineer

Athens, GA Β· On-site

$45 - $48/hr

Aseptic Manufacturing Validation Engineer Location: Athens, GA Type: 12 month contract Compensation ... equipment, utilities, and facilities. This role is responsible for qualification, protocol ...

Validation Engineer

Athens, GA Β· On-site

$45 - $48/hr

Aseptic Manufacturing Validation Engineer Location: Athens, GA Type: 12 month contract Compensation ... equipment, utilities, and facilities. This role is responsible for qualification, protocol ...

Showing results 41-60

Equipment Qualification Validation Engineer information

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How much do equipment qualification validation engineer jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for equipment qualification validation engineer in the United States is $63.77, according to ZipRecruiter salary data. Most workers in this role earn between $52.64 and $69.71 per hour, depending on experience, location, and employer.

What are popular job titles related to Equipment Qualification Validation Engineer jobs?

For Equipment Qualification Validation Engineer jobs, the most frequently searched job titles are:

Infographic showing various Equipment Qualification Validation Engineer job openings in the United States as of July 2026, with employment types broken down into 95% Full Time, 2% Part Time, and 3% Contract. Highlights an 87% Physical, 4% Hybrid, and 9% Remote job distribution, with an average salary of $132,650 per year, or $63.8 per hour.

Validation Engineer

Pleasant Prairie, WI β€’ On-site

Performance Validation, Inc
Pharmaceutical and Medicine ManufacturingΒ β€’Β 51 - 200 employees

$72K - $100K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 29 days ago


Key responsibilities

  • Develop verification and qualification deliverables such as Requirements Documents, Functional and Design Specifications, Test Protocols (IQ/OQ/PQ), and Summary Reports.

  • Execute test protocols and identify and resolve non-conformances or deviations.

  • Track and manage change control activities for multiple concurrent projects.


Job description

About Us
Here at Performance Validation, Inc (PV) we have been providing Commissioning, Qualification, and Validation services to the life science industries for 37 years. We are a 100% employee owned company with teams in Indiana, Michigan, Illinois, Kansas, Washington, Wisconsin, and North Carolina, and we support clients throughout the US and overseas. As an employer, PV is committed to providing growth opportunities to our employees through professional development, implementation of new services, and cultivation of new geographical areas.
About the job
Performance Validation is seeking a full-time Level 2 Validation Engineer/Specialist or Senior Validation Engineer to join our team in Pleasant Prairie, WI. The Level II/III Validation Engineer/Specialist reports directly to the Project Leader and will be assigned to one or more project teams headed by a Project Leader.
Responsibilities
  • Develop a sound understanding of how to properly implement technical, quality, and scientific principals necessary to meet industry and customer requirements
  • Work in a team environment to meet defined objectives based on established timelines
  • Develop verification/qualification deliverables including but not limited to Requirements Documents, Functional and Design Specifications, Test Protocols (IQ/OQ/PQ), and Summary Reports
  • Execute test protocols, including identification and resolution of non-conformances/deviations
  • Track and manage change control activities for multiple concurrent projects
Requirements you will need
Education:
  • BS/BA degree and minimum of 2 years in pharmaceutical or other regulated industry experience directly related to pharmaceutical validation
  • BS degrees in Biomedical Engineering, Chemical Engineering or Mechanical Engineering preferred

Experience:
  • Self-starter who exhibits a professional demeanor, enthusiasm, and ability to work independently with minimal supervision
  • Strong interpersonal skills. Must interact confidently with clients, other contractors, and employees
  • Possess excellent oral and written communication skills and high attention to detail
  • Experience with office word-processing and spreadsheet programs such as Microsoft Word and Excel

What we have to offer
  • Competitive base salary
  • Biannual profit share
  • Employee stock ownership program
  • 401(k) company match
  • Flexible time off policy
  • Paid Parental Leave
  • Internal and external training opportunities
  • Medical, vision, and dental coverage
  • Disability and life insurance
  • Cellphone stipend
  • Growth opportunities
  • Company-sponsored team building outings
  • A collaborative work environment
  • Work/life balance
This role involves frequent travel to client and partner sites, estimated at 30–50% depending on business needs and project cycles.

Please note that the salary range provided is a good faith estimate on the applicable range. The final salary offer will be determined after considering relevant factors, including a candidate's qualifications and experience, where appropriate.

Qualified candidates must be legally authorized to be employed in the United States. Performance Validation, Inc. does not anticipate providing sponsorship for employment visa status (e.g., H-1B status) for this employment position.