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Qa Validation Engineer Jobs in Massachusetts (NOW HIRING)

Aequor

Specialist QA - Validation, cGMP

Woburn, MA

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 ...

DataServ / xFact

QA Engineer

North Andover, MA · On-site

$115K - $120K/yr

... then validate and refine these outputs Help evaluate and adopt AI-powered QA tools (e.g., self ... one scripting/programming language (e.g., Python, JavaScript/TypeScript, or Java) Tools:

IT EXCEL LLC

Jr QA Tester

Cambridge, MA

$55K - $58K/yr

RELOCATION IS A MUST AND 4 WEEKS MANDATORY IN-PERSON TRAINING IN RESTON, VA Title: Jr. Validation Engineer/QA Analyst/ Jr. QA Tester/Business Analyst/BA Description : WE ARE LOOKING FOR FRESH ...

IT EXCEL LLC

Jr QA Tester

Cambridge, MA · On-site

$55K - $58K/yr

RELOCATION IS A MUST AND 4 WEEKS MANDATORY IN-PERSON TRAINING IN RESTON, VA Title: Jr. Validation Engineer/QA Analyst/ Jr. QA Tester/Business Analyst/BA Description : WE ARE LOOKING FOR FRESH ...

DataServ

QA Engineer

North Andover, MA · On-site

$115K - $120K/yr

... validate and refine these outputs • Help evaluate and adopt AI-powered QA tools (e.g., self ... scripting/programming language (e.g., Python, JavaScript/TypeScript, or Java) Tools: • ...

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Qa Validation Engineer information

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How much do qa validation engineer jobs pay per hour?

As of Aug 31, 2026, the average hourly pay for qa 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 a QA Validation Engineer?

QA Validation Engineers are professionals responsible for ensuring that products, systems, or software meet specified quality and regulatory standards before they are released or deployed. They design and execute validation protocols, document results, and identify any issues or non-conformities during the testing process. Their role is crucial in industries like pharmaceuticals, manufacturing, and software, where compliance and reliability are essential. QA Validation Engineers collaborate closely with development, production, and regulatory teams to ensure that products are safe, effective, and meet all necessary guidelines.

How does a QA Validation Engineer typically collaborate with cross-functional teams during product development?

As a QA Validation Engineer, you’ll work closely with development, regulatory, and operations teams to ensure products meet quality and compliance standards. You’ll participate in project meetings, review technical documentation, and provide input on test strategies and validation protocols. Effective communication and problem-solving are essential, as you may need to clarify requirements, address issues found during validation, and coordinate testing activities. This collaborative environment helps ensure that products are released on schedule and comply with industry regulations.

What are the key skills and qualifications needed to thrive as a QA Validation Engineer, and why are they important?

To thrive as a QA Validation Engineer, you need a solid understanding of quality assurance methodologies, validation protocols, and a relevant technical degree such as in engineering or life sciences. Familiarity with industry regulations (such as FDA or ISO standards), validation management software, and documentation tools is typically required. Attention to detail, analytical thinking, and strong communication skills help you excel in identifying compliance gaps and collaborating with cross-functional teams. These skills and qualities are crucial to ensure products meet regulatory requirements and maintain high standards of quality and safety.

What is the difference between Qa Validation Engineer vs QA Tester?

AspectQa Validation EngineerQA Tester
CertificationsISTQB, CQE, or similarISTQB Foundation, CSTE
Work EnvironmentRegulatory, validation-focused industries like pharma, biotechSoftware development, IT, web applications
ResponsibilitiesValidating systems, ensuring compliance, writing validation protocolsExecuting test cases, identifying bugs, reporting issues

While both roles focus on quality assurance, Qa Validation Engineers primarily work on validating systems for compliance and regulatory standards, often in industries like pharmaceuticals. QA Testers concentrate on testing software functionality and identifying bugs during development. The roles overlap in testing skills but differ in scope and industry focus.

Are QA Validation Engineers in demand?

QA Validation Engineers are in demand across industries such as pharmaceuticals, biotech, and manufacturing, where regulatory compliance and quality assurance are critical. The role requires knowledge of validation processes, testing protocols, and often involves working with tools like GxP standards and validation software, making experienced professionals highly sought after.

Do validation engineers make good money?

Validation engineers, including QA validation engineers, typically earn competitive salaries that vary by industry, experience, and location. They often require knowledge of testing tools, validation protocols, and quality standards, which can influence compensation levels. Overall, validation engineering is considered a well-paying profession within quality assurance and engineering fields.

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

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

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

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

What cities in Massachusetts are hiring for Qa Validation Engineer jobs?

Cities in Massachusetts with the most Qa Validation Engineer job openings:

Qa Validation Engineer jobs near you
Infographic showing various Qa Validation Engineer job openings in Massachusetts as of August 2026, with employment types broken down into 95% Full Time, 2% Part Time, and 3% Contract. Highlights an 85% Physical, 6% Hybrid, and 9% Remote job distribution, with an average salary of $118,116 per year, or $56.8 per hour.

Quality Assurance Validation Contractor

BioPharma Consulting JAD Group

Boston, MA • On-site

Contractor

Re-posted 23 days ago

Job description

We are looking for Quality Assurance Validation contractors to join our growing QA Validation group in Boston MA. Positions range from 6 to 12 months. The roles are expected to be onsite in Boston, MA.
Responsibilities:
  • Provide QA oversight of CQV activities for the cGMP manufacturing facility and quality control laboratories.
  • Provide QA oversight for periodic review and requalification program.
  • Perform review of CMMS records related to asset management including asset release, database requests, and work orders.
  • Author and perform review of SOPs in Veeva.
  • Review and approve validation protocols and reports (IQ, OQ, PQ, CSV, process validation, cleaning validation).
  • Ensure compliance of validation activities with applicable GMP regulations, industry guidance, and internal SOPs.
  • Collaborate with cross-functional teams (Validation, QA, Engineering, Manufacturing, QC) to support timely execution of validation projects.
  • Participate in change control assessments, risk assessments, and deviation investigations related to validation.
  • Provide QA input during validation planning and execution phases.
  • Support audits and regulatory inspections by providing validation documentation and addressing QA-related inquiries.
  • Ensure data integrity and documentation accuracy in all validation records.
  • Maintain cu

Requirements
  • Bachelor's degree in a technical discipline with 5+ years validation and/or quality assurance experience. In lieu of degree, 7+ years of equivalent work experience is required.
  • Knowledge of 21 CFR, ICH, EU Regulations, GAMP 5, risk-based validation.
  • Prior experience working in cell and gene therapy manufacturing preferred.
  • Prior experience working with contract manufacturing preferred.
  • Experience with Kneat strongly preferred.
  • Applies collaborative approach to problem solving and is experienced with risk-based decision making.
  • Team player who works well in large multi-disciplinary project groups by listening effectively and inviting open discussion.

Benefits
  • 6-12 month contract with possible extension
  • administrative shift

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