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Design Quality Engineer Jobs in Boston, MA (NOW HIRING)

Design Quality Engineer

Bedford, MA ยท On-site

$103K - $163K/yr

Job Title Design Quality Engineer The Design Quality Engineer is accountable for design quality, risk management, sustaining and complaint investigations for Philips Image Guided Therapy products.

Job TitleDesign Quality Engineer The Design Quality Engineer is accountable for design quality, risk management, sustaining and complaint investigations for Philips Image Guided Therapy products.

Lead Design Quality Engineer

Billerica, MA ยท On-site

$125K - $150K/yr

Lead Design Quality Assurance Engineer Billerica, Massachusetts Quanterix is revolutionizing biomarker analysis to advance precision health, leveraging Simoa technology for ultra-sensitive protein ...

Lead Design Quality Engineer

Billerica, MA ยท On-site

$125K - $150K/yr

The Lead Design Quality Assurance Engineer develops, establishes, and maintains quality engineering methodologies, systems, and practices which meet Quanterix, customer, and regulatory requirements.

Sr. Design Quality Engineer

Wilmington, MA ยท On-site

$96K - $131K/yr

Senior Design Quality Engineer (Medical Devices) - Multi-Portfolio Startup Location: US-based, Wilmington, MA (hybrid will be considered) Function: Quality Reports to: Head of Quality Management ...

Sr. Design Quality Engineer

Wilmington, MA ยท Hybrid

$96K - $131K/yr

Senior Design Quality Engineer (Medical Devices) - Multi-Portfolio Startup Location: US-based, Wilmington, MA(hybrid will be considered) Function: Quality Reports to: Head of Quality Management ...

Software Design Quality Engineer

Bedford, MA ยท On-site

$102K - $163K/yr

Job Title Software Design Quality Engineer The Software Design Quality Engineer is responsible for developing, maintaining, and managing comprehensive software quality documentation, ensuring their ...

Job TitleSoftware Design Quality Engineer The Software Design Quality Engineer is responsible for developing, maintaining, and managing comprehensive software quality documentation, ensuring their ...

Senior Design Quality Engineer

Cambridge, MA ยท On-site

$103K - $145K/yr

Job TitleSenior Design Quality Engineer In this role you Will be part of a team that is excited by the unique professional challenges that our Quality Transformation presents, has strong technical ...

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Design Quality Engineer information

See Boston, MA salary details

$20

$51

$75

How much do design quality engineer jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for design quality engineer in Boston, MA is $51.25, according to ZipRecruiter salary data. Most workers in this role earn between $42.02 and $61.35 per hour, depending on experience, location, and employer.

How does a design quality engineer typically collaborate with cross-functional teams during product development?

As a Design Quality Engineer, you work closely with teams such as R&D, manufacturing, regulatory affairs, and supply chain throughout the product development lifecycle. Your primary role is to ensure quality standards are integrated from the initial concept through to product launch. This often involves participating in design reviews, facilitating risk assessments like FMEA, and ensuring compliance with relevant regulations. Effective communication and problem-solving skills are essential, as you'll help bridge gaps between design intent and manufacturability to ensure a smooth transition to production.

What are the key skills and qualifications needed to thrive as a design quality engineer?

To thrive as a Design Quality Engineer, you need a solid background in engineering principles, quality assurance methodologies, and a relevant degree such as mechanical or electrical engineering. Familiarity with standards like ISO 13485 or ISO 9001, proficiency in tools such as FMEA, risk analysis software, and statistical analysis platforms like Minitab are typically required. Strong problem-solving abilities, attention to detail, and effective communication skills help distinguish top performers in this role. These skills ensure that products meet regulatory requirements, maintain high quality standards, and minimize risk throughout the design and development process.

What is a design quality engineer?

Design Quality Engineers are professionals who ensure that products are developed and manufactured according to quality standards and regulatory requirements. They work closely with design, engineering, and manufacturing teams to identify potential risks, implement quality controls, and validate product designs. Their goal is to make sure that products are safe, effective, and meet customer expectations before they are released to the market.

What is the difference between Design Quality Engineer vs Manufacturing Quality Engineer?

AspectDesign Quality EngineerManufacturing Quality Engineer
Primary FocusEnsuring product design meets quality standards and specifications during developmentMonitoring and improving quality in manufacturing processes and final products
Work EnvironmentDesign labs, R&D departments, product development teamsProduction lines, manufacturing plants, quality control departments
Required CredentialsBachelor's in Engineering, Quality certifications (e.g., CQE), knowledge of design standardsBachelor's in Engineering or Manufacturing, Quality certifications, process improvement skills

Design Quality Engineers focus on product design and development to prevent defects early, while Manufacturing Quality Engineers concentrate on maintaining quality during production. Both roles require similar credentials and work within quality assurance but target different stages of the product lifecycle.

Are design quality engineers well paid?

Design quality engineers typically earn competitive salaries that reflect their technical expertise in quality assurance, design review, and engineering standards. Salaries vary based on experience, industry, and location, but they are generally above average compared to other engineering roles. Certifications like Six Sigma or ISO standards can also influence compensation levels.
What are the most commonly searched types of Design Quality Engineer jobs in Boston, MA? The most popular types of Design Quality Engineer jobs in Boston, MA are:
What are popular job titles related to Design Quality Engineer jobs in Boston, MA? For Design Quality Engineer jobs in Boston, MA, the most frequently searched job titles are:
Infographic showing various Design Quality Engineer job openings in Boston, MA as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 14% Part Time, 5% Contract, and 1% Nights. Highlights an 90% Physical, 2% Hybrid, and 8% Remote job distribution, with an average salary of $106,607 per year, or $51.3 per hour.

Design Quality Engineer

Kanak Elite Services Inc

Andover, MA โ€ข On-site

Contractor

Posted 28 days ago


Job description

Hello There,
Please go through the below job description and revert me with your Updated Resume and  below details to fasten up the process. 

Email to : yashmita@kanakits.com


Visa-Status :
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ROLE : DESIGN QUALITY ENGINEER

TYPE : ONSITE IN ANDOVER, MA

DURATION : 3-MONTH CTH

INTERVIEW TYPE : VIDEO INTERVIEW

Job Description

As a Design Quality Engineer (DQE) for our medical device manufacturer client in the Greater Boston region, you will be responsible for ensuring end to end design quality and compliance across the product development lifecycle for Class II/III medical devices, including software-driven and active implantable products. Working directly with cross-functional teams, you will drive adherence to design controls, risk management, and SDLC best practices from concept through commercialization and post market activities.

Qualifications:

  • Bachelors degree in Engineering (Biomedical, Software, Systems) or a related technical discipline
  • Advanced degree (Masters) in Engineering, Quality, or Regulatory Affairs preferred
  • Relevant certifications (e.g., ASQ CQE, CSQE, Six Sigma Green/Black Belt) are a plus

Required Skills

  • 10+ years of experience in Quality Engineering supporting regulated medical device development (Class II/III preferred)
  • Strong hands on experience with design controls, DHF management, and traceability in regulated environments
  • Working knowledge of applicable standards and regulations (e.g., 21 CFR 820, ISO 13485, ISO 14971, IEC 62304)
  • Experience supporting software quality within the SDLC and understanding of software risk management principles
  • Proven experience with risk management tools (e.g., FMEA, hazard analysis) and integration into product development
  • Experience supporting audits and regulatory submissions, with the ability to defend design and quality documentation
  • Strong analytical, documentation, and communication skills with ability to work effectively across cross-functional teams
  • Experience with quality systems, eQMS/PLM tools, and defect/CAPA management processes

Key Responsibilities

  • Serving as the quality lead on product development teams, ensuring compliance with design controls across all lifecycle phases (planning, inputs/outputs, verification, validation, transfer, and change management)
  • Establishing and maintaining DHF, DMR, and DHR, ensuring complete traceability from user needs through verification and validation evidence
  • Leading and maintaining risk management activities (hazard analysis, FMEA, risk files) and ensuring integration of risk controls into design and validation activities
  • Providing quality oversight of software SDLC activities, ensuring compliance with applicable standards (e.g., IEC 62304) and integration with system-level risk management
  • Reviewing and approving design, software, and validation deliverables to ensure completeness, consistency, and audit readiness
  • Supporting verification, validation, and design transfer activities, ensuring alignment between design outputs and production processes
  • Leading or supporting CAPA, nonconformance investigations, and root cause analysis to drive continuous improvement
  • Supporting internal and external audits (FDA, Notified Body, ISO), and contributing to regulatory submissions (e.g., IDE, PMA, EU MDR)