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Qa Validation Jobs (NOW HIRING)

The Quality Assurance Manager , Validations is located in Chaska, MN and reports to the Director of Quality Assurance. Our analyzers and reagents are medical laboratory devices used to calculate the ...

... quality assurance in a cGMP-regulated environment. This individual will contribute to method development, validation, troubleshooting, and support project timelines while ensuring data integrity and ...

Company Description Engineering Job Title- Specialist QA Location- Woburn, MA Duration - 12 months with possible extension Key Skills - QA Pharma, Bio, biopharma, cGMP, validation, conformance, CAPAs ...

Validation QA Specialist

Pomona, CA · On-site

$110 - $120/hr

Your Role The Validation QA Specialist is responsible for providing Quality Assurance oversight of validation documentation and ensuring compliance with applicable GMP regulations, company procedures ...

Validation QA Specialist

Pomona, CA · On-site

$110K - $120K/yr

Your Role The Validation QA Specialist is responsible for providing Quality Assurance oversight of validation documentation and ensuring compliance with applicable GMP regulations, company procedures ...

Your Role The Validation QA Specialist is responsible for providing Quality Assurance oversight of validation documentation and ensuring compliance with applicable GMP regulations, company procedures ...

Your Role The Validation QA Specialist is responsible for providing Quality Assurance oversight of validation documentation and ensuring compliance with applicable GMP regulations, company procedures ...

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QA Validation information

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$10

$56

$98

How much do qa validation jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for qa validation in the United States is $56.31, according to ZipRecruiter salary data. Most workers in this role earn between $41.59 and $70.43 per hour, depending on experience, location, and employer.

What is a QA Validation professional?

QA Validation professionals are specialists responsible for ensuring that products, processes, or systems meet defined quality standards and regulatory requirements. They design and execute tests, document results, and analyze data to confirm that all specifications are met before a product is released or a process goes live. Their work is crucial in industries such as pharmaceuticals, manufacturing, and software, where compliance and consistent quality are essential. QA Validation experts help prevent defects, ensure safety, and maintain customer trust.

What are the key skills and qualifications needed to thrive as a QA Validation professional?

To thrive as a QA Validation professional, you need a solid understanding of quality assurance processes, regulatory standards (such as FDA or ISO), and a relevant science or engineering degree. Familiarity with validation protocols, documentation systems, and tools like LIMS or TrackWise is typically required, along with certifications such as ASQ CQV or similar. Attention to detail, analytical thinking, and effective communication are essential soft skills for ensuring compliance and facilitating teamwork. These competencies are critical for guaranteeing product quality, regulatory compliance, and the smooth operation of validation activities in highly regulated industries.

What are some common challenges faced by QA Validation professionals in regulated industries?

QA Validation professionals in regulated industries often face the challenge of staying current with evolving compliance standards while ensuring that all processes and documentation meet strict regulatory requirements. They must balance thorough validation activities with tight project timelines, often collaborating closely with cross-functional teams such as manufacturing, engineering, and regulatory affairs. Attention to detail and strong organizational skills are essential, as even small errors can lead to costly delays or regulatory findings. Effective communication with team members and stakeholders is also critical to ensure successful audits and product launches.

What is the difference between Qa Validation vs Qa Analyst?

AspectQa ValidationQa Analyst
CertificationsGMP, GxP, Validation certificationsGMP, GxP, Quality assurance certifications
Work EnvironmentRegulated industries like pharma, biotechPharmaceutical, biotech, manufacturing
Primary FocusValidating processes, systems, equipmentAnalyzing quality data, audits, process improvements
Employer UsageQuality validation teams in regulated industriesQuality assurance departments across industries

Qa Validation specialists focus on validating systems and processes to ensure compliance with industry standards, often working on equipment and software validation. Qa Analysts primarily analyze quality data, perform audits, and support process improvements. While both roles ensure product quality, Qa Validation emphasizes validation activities, whereas Qa Analysts focus on ongoing quality analysis and reporting.

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What cities are hiring for Qa Validation jobs?

Cities with the most Qa Validation job openings:

What are the most commonly searched types of Qa Validation jobs?

The most popular types of Qa Validation jobs are:

What states have the most Qa Validation jobs?

States with the most job openings for Qa Validation jobs include:

Infographic showing various Qa Validation job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 90% Full Time, 4% Part Time, and 5% Contract. Highlights an 84% Physical, 5% Hybrid, and 11% Remote job distribution, with an average salary of $117,123 per year, or $56.3 per hour.

Manager Quality Assurance, Validation

Danaher

Chaska, MN

$130K - $160K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 4 days ago


Danaher rating

7.7

Company rating: 7.7 out of 10

Based on 31 frontline employees who took The Breakroom Quiz

200th of 543 rated manufacturers


Job description

Bring more to life.

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?

At Beckman Coulter Diagnostics, one of Danaher's 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact.

You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life.

As a global leader in clinical diagnostics, Beckman Coulter Diagnostics has challenged convention to elevate the diagnostic laboratory's role in improving patient health for more than 90 years. Our diagnostic solutions are used in routine and complex clinical testing, and are used in hospitals, reference and research laboratories, and physician offices around the world. Every hour around the world, more than one million tests are run on Beckman Coulter Diagnostics systems, impacting 1.2 billion patients and more than three million clinicians per year. From uncovering the next clinical breakthrough, to rapid and reliable sample analysis, to more rigorous decision making-we are enabling clinicians to deliver the best possible care to their patients with improved efficiency, clinical confidence, adaptive collaboration, and accelerated intelligence.

Learn about the Danaher Business System which makes everything possible.

The Quality Assurance Manager, Validations is located in Chaska, MN and reports to the Director of Quality Assurance. Our analyzers and reagents are medical laboratory devices used to calculate the concentration of certain substances within samples of serum, plasma, urine and/or other body fluids. Substances analyzed through these instruments include certain metabolites, electrolytes, proteins, and/or drugs. The Quality Assurance Manager partners with the manufacturing operations and development teams to ensure delivery of high quality, reliable and compliant products.

This position will manage professional associates and operation support assigned to the Quality Assurance line support and validation team management, equipment program management, Design Change teams responsible for cost savings and supply continuity, including 7+ direct reports, instilling and sustaining a culture of Quality across the teams.

This role also includes the following opportunity to:

  • Develop objectives, measures progress against goals, and complete performance reviews for direct reports. Responsible for the performance and results of the teams.
  • Adapt departmental plans and priorities to address resource and operational challenges, working cross functionally with other managers to align site objectives, as needed.
  • Create an environment that attracts, develops, and retains high quality associates. Champion employee engagement, diversity, professional development and high levels of employee satisfaction.
  • Use policies, procedures and business/department plan to guide decisions and problem solving.

The essential requirements of the job include:

  • Bachelor's degree with 9+ years of experience or Master's degree with 7+ years of experience. (Degree preferably in Chemistry, Biology, or similar scientific field)
  • Previous management/supervisory or project management or leadership experience.
  • Requires in-depth understanding of concepts, theories and principles within Quality Systems, Process Validation, Test method validation and Manufacturing Quality disciplines and basic knowledge of other disciplines.
  • Experience with non-product software validation for manufacturing automation
  • Manufacturing process validation experience - medical device or pharmacy industry highly preferred
  • Experience with Quality System Regulation 21 CFR 820, Quality Management System ISO 13485:2016 and ISO 9001:2015


This experience is a plus:

  • Experience with equipment lifecycle management
  • Lead Auditor Certification

Beckman Coulter Diagnostics, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.

The annual salary range for this role is $130,000 to $160,000. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.

This job is also eligible for bonus/incentive pay.

We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law.

Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.

For more information, visit www.danaher.com.

Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law.

The U.S. EEO posters are available here.

We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:1-202-419-7762 or applyassistance@danaher.com.


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About Danaher

Sourced by ZipRecruiter

We are a science and technology innovator committed to helping our customers solve complex challenges, and improving quality of life around the world. A global family of more than 20 operating companies, we drive meaningful innovation in some of today's most dynamic, growing industries.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Washington, DC, US

Year founded

1984