ZipRecruiter

Log In

1

Validation Engineer Biomedical Jobs in Boston, MA

Elucid

Senior Clinical Validation Engineer

Boston, MA · On-site

$140K - $165K/yr

Degree in biomedical engineering or related field with 5+ years of SaMD validation or clinical QA experience. or, Advanced degree in a related field with 2+ years of relevant experience. * Excellent ...

Elucid

Senior Clinical Validation Engineer

Boston, MA · On-site

Degree in biomedical engineering or related field with 5+ years of SaMD validation or clinical QA experience. or, Advanced degree in a related field with 2+ years of relevant experience. * Excellent ...

Elucid

Senior Clinical Validation Engineer

Boston, MA · On-site

$140K - $165K/yr

Degree in biomedical engineering or related field with 5+ years of SaMD validation or clinical QA experience. or, Advanced degree in a related field with 2+ years of relevant experience. * Excellent ...

Fusion Life Sciences

CQV Engineer

Boston, MA · On-site

The Engineer is actively involved in Commissioning, Qualification, Validation, and Requalification ... Minimum Bachelor's degree in an Engineering (Chemical, Biomedical, Industrial, Biotechnology) or ...

next page

Showing results 1-20

All JobsValidation Engineer Biomedical JobsValidation Engineer Biomedical Jobs in Boston, MA

Validation Engineer Biomedical information

See Boston, MA salary details

$24

$56

$84

How much do validation engineer biomedical jobs pay per hour?

As of Sep 14, 2026, the average hourly pay for validation engineer biomedical in Boston, MA is $56.49, according to ZipRecruiter salary data. Most workers in this role earn between $42.84 and $68.70 per hour, depending on experience, location, and employer.

What does a validation engineer do in biomedical?

A Validation Engineer in the biomedical industry ensures that equipment, processes, and systems used in the production of medical devices or pharmaceuticals meet regulatory standards and function as intended. Their work involves planning and executing validation protocols, documenting results, and troubleshooting any deviations. This role is crucial for maintaining product quality, patient safety, and compliance with regulatory agencies such as the FDA. Validation Engineers often collaborate with quality assurance, manufacturing, and research teams to establish and maintain validated systems throughout a product's lifecycle.

What are the key skills and qualifications needed to thrive as a validation engineer in biomedical?

To thrive as a Validation Engineer in Biomedical, you need a solid background in engineering or life sciences, knowledge of regulatory standards (such as FDA or ISO 13485), and experience with validation protocols. Familiarity with technical tools like statistical analysis software, calibration equipment, and documentation systems is essential, and certifications such as Six Sigma or CQE can be advantageous. Strong problem-solving, attention to detail, and effective communication skills help you excel in cross-functional teams and ensure compliance. These skills are crucial for maintaining product quality, meeting regulatory requirements, and ensuring patient safety in biomedical environments.

What are some typical challenges faced by validation engineers in the biomedical industry and how can they be addressed?

Validation Engineers in the biomedical field often face challenges such as keeping up with evolving regulatory requirements, managing complex documentation, and ensuring equipment or processes meet stringent quality standards. Navigating audits and working cross-functionally with R&D, manufacturing, and quality assurance teams can also be demanding. To address these challenges, staying current with industry regulations, developing strong organizational and communication skills, and maintaining meticulous records are essential for success and career growth in this role.

What is the difference between Validation Engineer Biomedical vs Quality Assurance Engineer Biomedical?

AspectValidation Engineer BiomedicalQuality Assurance Engineer Biomedical
CertificationsGMP, ISO, FDA validation certificationsGMP, ISO, audit and compliance certifications
Work EnvironmentDesign, develop, and execute validation protocols for medical devicesDevelop and maintain quality systems, audits, and process improvements
Industry UsagePrimarily in medical device manufacturing and regulatory validationAcross medical device, pharmaceutical, and biotech industries

Validation Engineer Biomedical focuses on ensuring medical devices meet regulatory validation requirements through testing and protocols. Quality Assurance Engineer Biomedical emphasizes maintaining quality systems, compliance, and process improvements. Both roles are essential in the biomedical industry but serve different functions related to validation versus quality assurance.

What are popular job titles related to Validation Engineer Biomedical jobs in Boston, MA?

For Validation Engineer Biomedical jobs in Boston, MA, the most frequently searched job titles are:

What job categories do people searching Validation Engineer Biomedical jobs in Boston, MA look for?

The top searched job categories for Validation Engineer Biomedical jobs in Boston, MA are:

Validation Engineer Biomedical jobs near you
Infographic showing various Validation Engineer Biomedical job openings in Boston, MA as of September 2026, with employment types broken down into 1% Internship, 86% Full Time, 9% Part Time, and 4% Contract. Highlights an 83% Physical, 5% Hybrid, and 12% Remote job distribution, with an average salary of $117,497 per year, or $56.5 per hour.

Software Tool Verification and Validation Engineer

Newton, MA • On-site

Noblesoft Technologies
Software Development • 51 - 200 employees
Learn more about Noblesoft Technologiesexternal

Contractor

Re-posted 10 days ago

Job description

Job Title: Software Tool Verification and Validation Engineer
Location: Newton, MA
Job Summary
We are seeking a detail-oriented Software Tool Verification and Validation Engineer to ensure the reliability, accuracy, and compliance of software tools used in development and production environments. This role involves planning, executing, and documenting validation activities in accordance with industry standards and regulatory requirements
Key Responsibilities
 
  • Develop and execute verification and validation plans, protocols, and test cases for software and hardware tools.
  • Collaborate with cross-functional teams to define validation requirements.
  • Perform risk assessments and impact analyses for software changes.
  • Document verification and validation results and maintain traceability matrices.
  • Ensure compliance with relevant standards (e.g., FDA 21 CFR Part 11, ISO 13485, GAMP 5).
  • Support audits and inspections by providing validation documentation.
 
  • Test Planning and Design
  • Develop comprehensive test plans, test cases, and test scripts based on software requirements and design specifications.
  • Ensure test plans cover all functional and non-functional requirements, including performance, reliability, and security.
Test Execution
  • Execute manual and automated tests to identify software application defects.
  • Conduct regression testing to ensure existing functionalities remain unaffected by new changes.
  • Perform exploratory testing to uncover potential issues not identified by formal test cases.
Documentation and Reporting
  • Document test results, including detailed descriptions of defects and steps to reproduce them.
Collaboration
  • Work closely with software developers, and systems engineers, to understand software requirements and functionality.
  • Compliance and Standards
  • Ensure testing activities comply with relevant regulatory standards (e.g., FDA, ISO 13485, IEC 62304).
Qualifications
Education
Bachelor's degree in Computer Science, Software Engineering, Biomedical Engineering, or a related field.
Experience
  • Minimum of 7+ years of experience in software testing, preferably in the medical device industry.
  • Experience with testing tools and frameworks (e.g., ClearQuest, Jama).
  • Familiarity with regulatory standards and guidelines for medical devices (e.g., FDA 21 CFR Part 820, ISO 13485, IEC 62304)