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Quality Validation Engineer Jobs in Massachusetts

This role is responsible for ensuring compliance with internal quality standards and regulatory ... The Validation Engineer will play a key role in supporting operational readiness, tech transfer ...

At Syner-G, we enable our people to build careers that impact positively on their quality of life ... The Validation Engineer will play a key role in supporting operational readiness, tech transfer ...

At Syner-G, we enable our people to build careers that impact positively on their quality of life ... The Validation Engineer will be responsible for driving overall quality performance and compliance ...

At Syner-G, we enable our people to build careers that impact positively on their quality of life ... The Validation Engineer will be responsible for driving overall quality performance and compliance ...

At Syner-G, we enable our people to build careers that impact positively on their quality of life ... The Validation Engineer will play a key role in supporting operational readiness, tech transfer ...

Validation Engineer

Chelsea, MA ยท On-site

$89K - $110K/yr

The Validation Engineer is responsible for executing validation activities within a GMP ... Quality Assurance to ensure timely and compliant resolution, including validation-related ...

The Validation Engineer will be responsible for driving overall quality performance and compliance throughout the organization by defining, implementing, and maintaining the validation program. KEY ...

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Showing results 1-20

Quality Validation Engineer information

See Massachusetts salary details

$24

$56

$85

How much do quality validation engineer jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for quality validation engineer in Massachusetts is $56.79, according to ZipRecruiter salary data. Most workers in this role earn between $43.08 and $69.04 per hour, depending on experience, location, and employer.

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.

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 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.

Do quality validation engineers make good money?

Quality validation engineers typically earn competitive salaries that vary based on experience, industry, and location. They often require skills in testing methodologies, quality assurance tools, and sometimes certifications like ISTQB, which can influence earning potential.

What are popular job titles related to Quality Validation Engineer jobs in Massachusetts?

For Quality Validation Engineer jobs in Massachusetts, the most frequently searched job titles are:

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

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

Infographic showing various Quality Validation Engineer job openings in Massachusetts as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 13% Part Time, 3% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $118,116 per year, or $56.8 per hour.

Validation Engineer

Stark Pharma Solutions Inc

Springfield, MA โ€ข On-site

Contractor

Re-posted 20 days ago


Job description

Hi,

My name is Sravani Dasari from Stark Pharma Solutions Inc. We are hiring talent for our client and are currently working on a Validation Engineer position. Please send me your updated resume if you have relevant experience and are interested in this opportunity. The detailed job description is as follows.

Job Title: Validation Engineer
Location: Massachusetts
Duration: Long Term

Position Overview

We are seeking an experienced Validation Engineer to support qualification and validation activities within a pharmaceutical manufacturing environment. This role will focus on equipment qualification, process validation, cleaning validation, computerized system validation, documentation review, and compliance with FDA and cGMP requirements. The ideal candidate will work closely with Manufacturing, Engineering, Quality Assurance, and Regulatory teams to ensure validated systems remain compliant and inspection-ready.

Key Responsibilities

• Develop, execute, and review validation protocols and reports, including IQ, OQ, PQ, and requalification activities.
• Support equipment, utility, facility, process, and cleaning validation programs.
• Prepare and maintain validation documentation in accordance with cGMP and regulatory requirements.
• Coordinate validation activities with Manufacturing, Engineering, Quality Assurance, and project teams.
• Perform risk assessments and gap analyses to identify validation and compliance requirements.
• Investigate validation deviations, implement corrective actions, and support CAPA activities.
• Ensure validation lifecycle activities comply with FDA regulations, 21 CFR Part 210/211, and industry standards.
• Support commissioning and qualification activities for new equipment, facilities, and manufacturing processes.
• Participate in audits, inspections, and validation-related regulatory submissions.
• Contribute to continuous improvement initiatives to enhance validation processes and compliance.

Required Qualifications

• Bachelor's Degree in Engineering, Pharmaceutical Sciences, Biotechnology, Chemistry, Life Sciences, or a related technical discipline.
• 3–7+ years of Validation Engineering experience within pharmaceutical, biotechnology, medical device, or regulated manufacturing environments.
• Strong experience with equipment qualification (IQ/OQ/PQ), process validation, and validation lifecycle management.
• Knowledge of cGMP regulations, FDA requirements, data integrity principles, and validation industry standards.
• Experience supporting cleaning validation, computerized system validation (CSV), or utility validation is preferred.
• Familiarity with risk assessments, deviation investigations, CAPA, and change control processes.
• Strong technical writing, documentation, analytical, and problem-solving skills.
• Ability to manage multiple validation projects and work effectively in a cross-functional environment.
• Experience supporting regulatory inspections and audit readiness activities is highly preferred.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.

Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/