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Qa Validation Engineer Jobs (NOW HIRING)

Ceva Santé Animale

QA Validation Engineer

Lenexa, KS · On-site

QA Validation Engineer The success of a company depends on the passionate people we partner with. Together, let's share our talents. As a global leader in animal health, Ceva Animal Health believes ...

Intellectt INC

QA Validation Specialist

Rensselaer, NY · On-site

The QA Validation Specialist will support facilities compliance and quality assurance activities by reviewing technical documentation, validating data, and ensuring adherence to regulatory standards ...

Intellectt INC

QA Validation Specialist

Rensselaer, NY · On-site

The QA Validation Specialist will support facilities compliance and quality assurance activities by reviewing technical documentation, validating data, and ensuring adherence to regulatory standards ...

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Qa Validation Engineer information

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How much do qa validation engineer jobs pay per hour?

As of Jul 31, 2026, the average hourly pay for qa 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.

What is the difference between Qa Validation Engineer vs QA Tester?

AspectQa Validation EngineerQA Tester
CertificationsISTQB, CQE, or similarISTQB Foundation, CSTE
Work EnvironmentRegulatory, validation-focused industries like pharma, biotechSoftware development, IT, web applications
ResponsibilitiesValidating systems, ensuring compliance, writing validation protocolsExecuting test cases, identifying bugs, reporting issues

While both roles focus on quality assurance, Qa Validation Engineers primarily work on validating systems for compliance and regulatory standards, often in industries like pharmaceuticals. QA Testers concentrate on testing software functionality and identifying bugs during development. The roles overlap in testing skills but differ in scope and industry focus.

How does a QA Validation Engineer typically collaborate with cross-functional teams during product development?

As a QA Validation Engineer, you’ll work closely with development, regulatory, and operations teams to ensure products meet quality and compliance standards. You’ll participate in project meetings, review technical documentation, and provide input on test strategies and validation protocols. Effective communication and problem-solving are essential, as you may need to clarify requirements, address issues found during validation, and coordinate testing activities. This collaborative environment helps ensure that products are released on schedule and comply with industry regulations.

What are QA Validation Engineers?

QA Validation Engineers are professionals responsible for ensuring that products, systems, or software meet specified quality and regulatory standards before they are released or deployed. They design and execute validation protocols, document results, and identify any issues or non-conformities during the testing process. Their role is crucial in industries like pharmaceuticals, manufacturing, and software, where compliance and reliability are essential. QA Validation Engineers collaborate closely with development, production, and regulatory teams to ensure that products are safe, effective, and meet all necessary guidelines.

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

To thrive as a QA Validation Engineer, you need a solid understanding of quality assurance methodologies, validation protocols, and a relevant technical degree such as in engineering or life sciences. Familiarity with industry regulations (such as FDA or ISO standards), validation management software, and documentation tools is typically required. Attention to detail, analytical thinking, and strong communication skills help you excel in identifying compliance gaps and collaborating with cross-functional teams. These skills and qualities are crucial to ensure products meet regulatory requirements and maintain high standards of quality and safety.
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What cities are hiring for Qa Validation Engineer jobs? Cities with the most Qa Validation Engineer job openings:
What states have the most Qa Validation Engineer jobs? States with the most job openings for Qa Validation Engineer jobs include:
What job categories do people searching Qa Validation Engineer jobs look for? The top searched job categories for Qa Validation Engineer jobs are:
Qa Validation Engineer jobs near you
Infographic showing various Qa Validation Engineer job openings in the United States as of July 2026, with employment types broken down into 96% Full Time, 1% Part Time, and 3% Contract. Highlights an 87% Physical, 5% Hybrid, and 8% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

QA Validation Engineer

Ceva Santé Animale

Lenexa, KS • On-site

Full-time

Re-posted 21 days ago

Job description

QA Validation Engineer
The success of a company depends on the passionate people we partner with.
Together, let's share our talents.
As a global leader in animal health, Ceva Animal Health believes our success is linked to our passionate people researching, developing , producing and supplying innovative health solutions for all animals, which contributes to the future of our diverse planet.
We are committed to ensuring the highest possible level of care and well-being for farm animals (poultry, pigs, ruminants), companion animals (dogs and cats) and wildlife.
Indeed, Our "Together, Beyond Animal Health" vision emphasizes that the health and wellbeing of people, animals and our planet are totally interlinked. More than ever, Ceva is committed to a "One Health" approach.
As part of our "Diversity, Equity and Inclusion" policy, Ceva Animal Heath is committed to the employment of people with disabilities and will make reasonable accommodations throughout the interview process to ensure an inclusive and accessible experience for all applicants. To request an accommodation, please contact a member of the Ceva Talent Acquisition team.
Yourmissions :
Location: Lenexa, KS
Job Summary and Purpose
The QA Validation Engineer in Lenexa, KS leads, designs, performs, and reports validation activities on processes, equipment, and systems used in the manufacture of regulated veterinary vaccines for domestic and international markets.
Responsibilities and Key Duties
  • Prepare and execute protocols including Cycle Development, Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), Engineering Studies (ES), Factory Acceptance Test (FAT), and Site Acceptance Test (SAT).
  • Review protocol drafts and resolve conflicts or concerns to achieve management pre-approval. Coordinate qualification execution and all aspects of validation projects with Operations, Engineering, Quality Control, and Quality Assurance.
  • Perform or supervise protocol execution and maintain documentation in compliance with current Good Documentation Practices (GDP). Review, analyze, and compile protocol data and write reports for management review and approval.
  • Perform and document risk assessments to determine validation strategy and approach. Execute re-qualification (RQ) studies and periodic reviews to ensure equipment, systems, and processes remain in a validated state.
  • Support and participate in change control processes for qualified and validated equipment, including refrigerators, freezers, incubators, autoclaves, lyophilizers, bioreactors, fermenters, ovens, ampule filling machines, and related systems. Maintain full understanding of applicable change control procedures.
  • Provide input to, review, and approve User Requirements Specifications (URS). Write, review, and edit standard operating procedures (SOPs) to align with validation requirements.
  • Provide input to Engineering on the preparation and execution of Factory Acceptance Tests (FAT) and Site Acceptance Tests (SAT).
  • Research equipment and processes to establish parameters and testing methods that meet validation requirements. Support the development of Validation Plans and Schedules.
  • Ensure processes and products comply with all local, state, and federal regulations. Oversee CGMP compliance and establish systems that identify opportunities for improvement and recommend changes to improve process effectiveness and quality.
  • Perform all other duties as assigned.
Technical / Functional Competencies
  • Ability to perform internal and study audits as a lead and participate in external audits as a member of the audit team
  • Knowledge of pharmaceutical development, regulatory requirements, and manufacturing sciences with a global perspective
  • Knowledge of quality systems tools with the ability to adapt them to organizational needs and global regulatory requirements (GLP, GCP, GMP)
  • Ability to validate Excel file programming according to defined objectives
  • Proficiency in the use of data logging equipment and instruments
  • Experience performing risk assessments, investigations, CAPAs, and Aseptic Process Simulations (APS or media fills) preferred
Education
  • Bachelor's degree in Engineering, Biotechnology, Biology, or Microbiology with 4+ years of validation experience in a biotech, biological, pharmaceutical, or other GMP-regulated industry
    OR
  • Master's degree in Engineering, Biotechnology, Biology, or Microbiology with 2+ years of validation experience in a biotech, biological, pharmaceutical, or other GMP-regulated industry
Physical Requirements
  • Ability to read, write legibly, and communicate in English
  • Visual inspection capability
  • Occasional lifting up to 25 pounds
  • Tasks frequently require prolonged mental and visual concentration
Travel Required
  • None

This job description is intended to convey information essential to understanding the scope, general nature, and level of work performed by job holders. It is not intended to be an exhaustive list of qualifications, skills, duties, responsibilities, or working conditions, nor does it constitute an employment contract. Ceva reserves the right to modify job duties and/or job descriptions at any time to meet business needs.
*VEVRAA Federal Contractor
**Ceva is an equal opportunity employer and all qualified applicants will be considered for employment without regard to race, color, religion, sex, national origin, age, genetic information, actual or perceived sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law. Ceva encourages men and women, members of all racial and ethnic groups, individuals with disabilities and veterans to apply.
669B
Yourprofile :
Education - Bachelor's degree in Engineering, Biotechnology, Biology, or Microbiology with 4+ years of validation work experience in biotech, biological, pharmaceutical or other GMP-regulated industry
OR
Master's degree in Engineering, Biotechnology, Biology, Microbiology with 2+ years of validation work experience in the biotech, biological, pharmaceutical or other GMP-regulated industry required.

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