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Quality Validation Engineer Jobs (NOW HIRING)

Position: Jr. Validation Engineer Location : St. Louis, MO Contract type: Contract Description ... Software quality/validation training Additional Information All your information will be kept ...

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How much do quality validation engineer jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for quality 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 a quality validation engineer?

A Quality Validation Engineer is a professional responsible for ensuring that products, systems, or processes meet established quality standards and regulatory requirements. They design and execute validation protocols, analyze test data, and document results to confirm that products are safe, effective, and compliant. Their work is crucial in industries like pharmaceuticals, manufacturing, and medical devices, where product quality and safety are paramount. Quality Validation Engineers collaborate with cross-functional teams to identify improvements and prevent defects, ensuring consistent product quality throughout the development and production processes.

How does a quality validation engineer typically collaborate with cross-functional teams to ensure product quality?

Quality Validation Engineers work closely with teams such as product development, manufacturing, and regulatory affairs to ensure that products meet established quality standards before release. They participate in design reviews, provide input on test protocols, and analyze data from validation studies. Effective communication and teamwork are essential, as the role often involves coordinating validation activities and addressing issues that arise across departments. This collaborative approach helps identify potential quality concerns early and ensures smooth implementation of corrective actions.

What are the key skills and qualifications needed to thrive as a quality validation engineer, and why are they important?

To thrive as a Quality Validation Engineer, you need a solid background in engineering or life sciences, knowledge of validation protocols, and experience with regulatory compliance standards such as GMP or ISO. Familiarity with validation software tools, data analysis systems, and documentation management platforms is typically required, along with certifications like CQE or CQA being advantageous. Strong attention to detail, analytical thinking, and effective communication skills help ensure thorough validation processes and collaboration across teams. These competencies are vital to maintaining product quality, meeting regulatory requirements, and minimizing risks in manufacturing or product development environments.

What is the difference between Quality Validation Engineer vs Quality Assurance Engineer?

AspectQuality Validation EngineerQuality Assurance Engineer
Primary FocusValidating products meet specifications through testing and validation processesDeveloping and implementing processes to ensure quality standards are maintained
Work EnvironmentLaboratories, testing facilities, manufacturing sitesOffice settings, process development, audits
CertificationsISO 9001, Six Sigma, CQE often preferredISO 9001, Six Sigma, CQE often preferred

Both roles focus on quality but differ in scope: Validation Engineers concentrate on testing and validating products, while Assurance Engineers develop processes to prevent defects. Understanding these differences helps in choosing the right career path or job focus.

Are quality validation engineers paid well?

Quality validation engineers typically earn competitive salaries that reflect their specialized skills in testing, validation, and quality assurance processes. Compensation varies based on experience, industry, and location, but they generally receive higher-than-average pay compared to entry-level roles in manufacturing or software testing. Certifications such as ISTQB or Six Sigma can also enhance earning potential.

Do quality validation engineers make good money?

Quality validation engineers typically earn competitive salaries that vary by industry, location, and experience level. They often require skills in testing methodologies, quality assurance tools, and sometimes certifications like ISTQB, which can influence earning potential.
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Infographic showing various Quality Validation Engineer job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 88% Physical, 1% Hybrid, and 11% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

Validation Engineer

Barceloneta, PR • On-site

Full-time

Re-posted 17 days ago


Key responsibilities

  • Develop, review, and execute validation protocols for aseptic filling lines, lyophilization, and support equipment.

  • Perform process validation activities related to sterile manufacturing, including media fills, and support commissioning and qualification activities for new equipment and facility upgrades.

  • Investigate deviations, CAPAs, and implement corrective actions related to validation activities.


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

Description:
We are seeking a Validation Engineer with hands-on experience in biotech/pharmaceutical manufacturing, specifically supporting aseptic filling operations (vials). This role will be responsible for executing and supporting validation activities for equipment, processes, and computerized systems in compliance with regulatory requirements and industry standards.
Responsibilities:
  • Develop, review, and execute validation protocols including IQ, OQ, PQ for:
    • Aseptic filling lines (vial filling, stoppering, capping)
    • Lyophilization (if applicable)
    • Support equipment (autoclaves, washers, depyrogenation tunnels)
  • Perform process validation activities related to sterile manufacturing, including media fills (APS).
  • Ensure compliance with cGMP, FDA, EMA, and ICH guidelines.
  • Support commissioning and qualification (C&Q) activities for new equipment and facility upgrades.
  • Generate and review:
    • Validation master plans (VMPs)
    • SOPs, protocols, and final reports
  • Collaborate with cross-functional teams (Manufacturing, QA, Engineering, MSAT).
  • Investigate deviations, CAPAs, and implement corrective actions related to validation activities.
  • Support risk assessments (FMEA, impact assessments) for validation scope.
  • Ensure data integrity and adherence to 21 CFR Part 11 requirements (if applicable to systems).

Qualifications:
  • Bachelor's degree in Engineering, Chemistry, Biology, or related field.
  • 3�7+ years of validation experience in biotech or pharmaceutical industry.
  • Strong experience with:
    • Aseptic processing
    • Vial filling operations
    • Sterile manufacturing environments
  • Must be fully bilingual (English / Spanish) with excellent oral skills.
  • Must be proficient using MS Windows and Microsoft Office applications.
  • Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.
  • Experience in Design Documentation (URS, DS), IQ, OQ, PQ protocols development and execution, deviations and reports generation.
  • Available to work extended hours, possibility of weekends and holidays.

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.