ZipRecruiter

Log In

1

Quality Validation Engineer Jobs (NOW HIRING)

Nemera

Quality Engineer - Validation

Buffalo Grove, IL · On-site

$73K - $95K/yr

The Quality Validation Engineer is responsible for planning, coordinating and managing through completion, assigned projects to ensure the development and production of products meets customer and ...

Nemera

Quality Engineer - Validation

Buffalo Grove, IL

$73K - $95K/yr

The Quality Validation Engineer is responsible for planning, coordinating and managing through completion, assigned projects to ensure the development and production of products meets customer and ...

New

Nemera

Quality Engineer - Validation

Buffalo Grove, IL

$73K - $95K/yr

The Quality Validation Engineer is responsible for planning, coordinating and managing through completion, assigned projects to ensure the development and production of products meets customer and ...

Nemera

Quality Engineer - Validation

Buffalo Grove, IL · On-site

$73K - $95K/yr

The Quality Validation Engineer is responsible for planning, coordinating and managing through completion, assigned projects to ensure the development and production of products meets customer and ...

Nemera

Quality Engineer - Validation

Buffalo Grove, IL

$73K - $95K/yr

The Quality Validation Engineer is responsible for planning, coordinating and managing through completion, assigned projects to ensure the development and production of products meets customer and ...

previous pagenext page

Showing results 21-40

All JobsTechnology JobsSoftware JobsSoftware Developer JobsQuality Validation Engineer Jobs

Quality Validation Engineer information

See salary details

$22

$51

$78

How much do quality validation engineer jobs pay per hour?

As of Aug 18, 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:

What job categories do people searching Quality Validation Engineer jobs look for?

The top searched job categories for Quality Validation Engineer jobs are:

Quality Validation Engineer jobs near you
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.

Calibration and Metrology Quality Validation Engineer

Thermo Fisher Scientific

Saint Louis, MO

$67K - $87K/yr

Full-time

Re-posted 2 days ago

Thermo Fisher Scientific rating

7.7

Company rating: 7.7 out of 10

Based on 427 frontline employees who took The Breakroom Quiz

199th of 540 rated manufacturers

Job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office

Job Description

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
DESCRIPTION:
As a Quality Engineer III, you'll help ensure quality excellence and regulatory compliance across manufacturing operations. You'll help ensure our products meet the highest standards while supporting our mission to enable customers to make the world healthier, cleaner, and safer. This role combines technical expertise with quality oversight to maintain robust quality management systems, lead investigations, drive continuous improvement, and ensure GMP/ISO compliance.
You'll work with multiple teams to resolve quality issues, conduct validation and equipment-based risk assessments, manage CAPAs, support audits, and implement quality initiatives. The role requires strong analytical and communication skills to interface effectively with internal teams and external customers/regulators. You'll help establish and maintain quality standards while supporting a culture of continuous improvement and compliance.
REQUIREMENTS:
• Advanced Degree plus 3 years of experience, or Bachelor's Degree plus 5 years of experience in quality assurance in regulated industry (pharmaceutical, medical device, or biotech)
• Preferred Fields of Study: Engineering, Life Sciences, Chemistry or related technical field
• ASQ certifications (CQE, CQA) desired
• Strong knowledge of cGMP, ISO 13485/9001, and applicable regulatory requirements (FDA, EMA, etc.)
• Expertise in quality systems including:

• Quality oversight of Calibrations and Metrology

• SAP knowledge a plus
• CAPA and deviation management
• Change control
• Risk management and FMEA
• Document control
• Internal/external auditing
• Advanced problem-solving and root cause analysis skills
• Excellent project management abilities
• Strong verbal and written communication skills
• Proficiency with quality management software and MS Office
• Experience with validation and qualification protocols
• Knowledge of statistical analysis and quality tools
• Ability to work both independently and collaboratively
• Strong attention to detail while maintaining broad perspective
• Excellent interpersonal skills for cross-functional collaboration
• May require up to 25% travel
• Additional language skills may be beneficial

Benefits

We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!

Other

Relocation assistance is not provided.

Must be legally authorized to work in the United States now and in the future, without sponsorship.

Must be able to pass a comprehensive background check, which includes a drug screening.

What Thermo Fisher Scientific employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Apply