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Quality Validation Engineer Jobs (NOW HIRING)

Requires a minimum of 8 years of quality, validation, or engineering experience in non-sterile clinical and commercial pharmaceutical manufacturing * Fundamental understanding of process equipment ...

Requires a minimum of 8 years of quality, validation, or engineering experience in non-sterile clinical and commercial pharmaceutical manufacturing * Fundamental understanding of process equipment ...

Requires a minimum of 8 years of quality, validation, or engineering experience in non-sterile clinical and commercial pharmaceutical manufacturing * Fundamental understanding of process equipment ...

Collaborate with Engineering, Quality Assurance, Manufacturing, Automation, Facilities, and other project stakeholders. * Track validation deliverables, schedules, open items, and project milestones.

New

Collaborate with Engineering, Quality Assurance, Manufacturing, Automation, Facilities, and other project stakeholders. * Track validation deliverables, schedules, open items, and project milestones.

Collaborate with Engineering, Quality Assurance, Manufacturing, Automation, Facilities, and other project stakeholders. * Track validation deliverables, schedules, open items, and project milestones.

New

Collaborate with Engineering, Quality Assurance, Manufacturing, Automation, Facilities, and other project stakeholders. * Track validation deliverables, schedules, open items, and project milestones.

New

Collaborate with Engineering, Quality Assurance, Manufacturing, Automation, Facilities, and other project stakeholders. * Track validation deliverables, schedules, open items, and project milestones.

New

Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions ... Ensure compliance with all safety regulations and quality policies, procedures, and GMP standards.

Validation Engineer IV

Rockville, MD · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Quality Agents, LLC is a service company offering validation and quality expertise to the pharmaceutical and biotechnology industries. Our Validation Engineers will be involved with the qualification ...

Validation Engineer

Tucson, AZ · On-site

$39 - $42/hr

  • Medical

  • Dental

  • Vision

... Quality, Design Transfer Operations, and other departments to resolve validation issues and ... What we are looking for in a Validation Engineer: · Bachelor's Degree in Engineering or Life ...

Collaborate with Engineering, Quality Assurance, Manufacturing, Automation, Facilities, and other project stakeholders. * Track validation deliverables, schedules, open items, and project milestones.

New

Validation Engineer II

Rockville, MD · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Quality Agents, LLC is a service company offering validation and quality expertise to the pharmaceutical and biotechnology industries. Our Validation Engineers will be involved with the qualification ...

Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions ... Ensure compliance with all safety regulations and quality policies, procedures, and GMP standards.

Showing results 41-60

Quality Validation Engineer information

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$51

$78

How much do quality validation engineer jobs pay per hour?

As of Aug 17, 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.
More about Quality Validation Engineer jobs

What cities are hiring for Quality Validation Engineer jobs?

Cities with the most Quality Validation Engineer job openings:

What states have the most Quality Validation Engineer jobs?

States with the most job openings for Quality Validation Engineer jobs include:

Infographic showing various Quality Validation Engineer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, 4% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

Validation Engineer

Sterling Engineering Inc.

Buffalo Grove, IL • On-site

$55 - $65/hr

Full-time

Re-posted 29 days ago


Job description

Validation Engineer – Injection Molding
Location: Buffalo Grove Il
Hire Type: Contract
Shift: 1st Shift | Monday–Friday
Compensation: $55–$65/hour
Overview
We are seeking a hands-on Validation Engineer with experience supporting plastic injection molding manufacturing within a regulated environment. This individual will lead equipment, process, and manufacturing validations while partnering closely with Manufacturing Engineering, Quality, Operations, and Automation teams to ensure new and existing molding processes meet quality and regulatory requirements.
The ideal candidate will have experience developing and executing IQ/OQ/PQ protocols, validating injection molding equipment and processes, troubleshooting manufacturing issues, and supporting continuous improvement initiatives in a medical device, pharmaceutical, or similarly regulated manufacturing environment.
Key Responsibilities
Develop, execute, and approve IQ, OQ, and PQ validation protocols for injection molding equipment, automation, and manufacturing processes.
Lead validation activities for new product introductions, equipment installations, process transfers, and manufacturing changes.
Validate injection molding processes including process windows, machine qualifications, tooling, auxiliary equipment, and automation systems.
Perform risk assessments utilizing FMEA and other risk management tools.
Investigate validation failures, process deviations, and nonconformances while implementing effective corrective actions.
Analyze process capability, statistical data, and validation results to ensure robust manufacturing processes.
Collaborate with Manufacturing Engineering to optimize molding parameters, cycle times, and process performance.
Support mold qualifications, process characterization, and production readiness activities.
Prepare validation reports, technical documentation, protocols, and supporting engineering documentation.
Participate in equipment FAT/SAT activities when applicable.
Ensure validation documentation complies with FDA, ISO 13485, GMP, and internal quality standards.
Support CAPA investigations, change control activities, and regulatory audits.
Work cross-functionally with Engineering, Quality, Production, Tooling, Automation, and Regulatory Affairs teams.

Qualifications

Bachelor's degree in Engineering or related technical discipline.
3+ years of validation engineering experience within a manufacturing environment.
Hands-on experience validating plastic injection molding processes and equipment.
Strong knowledge of IQ/OQ/PQ methodologies and validation lifecycle documentation.
Experience with process validation, equipment qualification, and manufacturing process development.
Familiarity with scientific molding principles and process optimization.
Experience with statistical analysis tools and process capability studies.
Knowledge of risk management methodologies including PFMEA/FMEA.
Strong technical writing and documentation skills.

Preferred Qualifications

Medical device, pharmaceutical, or highly regulated manufacturing experience.
Experience with automated manufacturing equipment, robotics, vision systems, and PLC-controlled equipment.
Knowledge of FDA 21 CFR Part 820, ISO 13485, GMP, and GAMP guidance.
Experience with injection mold qualification, tooling validation, and mold transfers.
Familiarity with cleanroom manufacturing environments.
Experience supporting CAPA, NCR investigations, and change control processes.
Working knowledge of Minitab or other statistical software.

Qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or genetic information.