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Principal Design Quality Engineer Jobs (NOW HIRING)

Senior Design Quality Engineer

Irvine, CA · On-site

$95K - $128K/yr

Provide quality engineering leadership for verification, validation, and design transfer activities ... U.S. work authorization sponsorship is not offered below Principal level * For Baccalaureate ...

Design Quality Engineer

Plano, TX · On-site

$40 - $45/hr

Design Quality Engineer Location: Plano, TX (onsite) Customer: Abbott Laboratories JD: * 6+ years of Medical devices - Design Quality experience for the projects related to Design Change, Clinical ...

The Design Quality Engineer will support critical quality activities throughout the medical device product development lifecycle, ensuring strict adherence to regulatory and quality requirements.

Design Quality Engineer - Plymouth, MN - Hybrid Daikin Applied is seeking a Design Quality Engineer responsible for ensuring product quality is designed, validated, and verified throughout the ...

Design Quality Engineer - Plymouth, MN - Hybrid Daikin Applied is seeking a Design Quality Engineer responsible for ensuring product quality is designed, validated, and verified throughout the ...

Design Quality Engineer - Plymouth, MN - Hybrid Daikin Applied is seeking a Design Quality Engineer responsible for ensuring product quality is designed, validated, and verified throughout the ...

Job Summary We are seeking a driven and results-oriented Design Quality Engineer to support product quality throughout the entire product lifecycle, from new product development and validation to ...

Showing results 21-40

Principal Design Quality Engineer information

See salary details

$64.5K

$125.5K

$171K

How much do principal design quality engineer jobs pay per year?

As of Sep 12, 2026, the average yearly pay for principal design quality engineer in the United States is $125,478.00, according to ZipRecruiter salary data. Most workers in this role earn between $102,500.00 and $150,000.00 per year, depending on experience, location, and employer.

What does a principal design quality engineer do?

A Principal Design Quality Engineer is responsible for ensuring that products are designed and developed in compliance with regulatory standards and internal quality requirements. They lead quality assurance activities throughout the product development lifecycle, including risk management, design verification and validation, and process improvements. These professionals collaborate with cross-functional teams to identify and resolve quality issues, mentor junior engineers, and support audits and inspections. Their expertise helps organizations deliver safe, effective, and reliable products to market.

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

To thrive as a Principal Design Quality Engineer, you need a deep understanding of design control, risk management, and quality systems, typically backed by a relevant engineering degree and substantial experience in regulated industries. Familiarity with ISO 13485, FDA 21 CFR Part 820, and statistical analysis tools like Minitab is essential, along with certifications such as CQE or Six Sigma. Outstanding problem-solving, leadership, and cross-functional communication skills make someone stand out in this role. These competencies are crucial for ensuring product safety, regulatory compliance, and continuous improvement in product design and development.

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

A Principal Design Quality Engineer plays a key role in bridging quality standards and engineering objectives by working closely with product development, regulatory, and manufacturing teams. They regularly participate in design reviews, risk assessments, and process validations, ensuring that quality is integrated at every stage. Their expertise helps resolve complex quality issues, influence design decisions, and mentor team members on compliance and best practices. This collaborative approach not only fosters a culture of quality but also drives product excellence and regulatory compliance.

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

AspectPrincipal Design Quality EngineerDesign Quality Engineer
CredentialsTypically requires a Bachelor's or Master's in Engineering, Quality Management certifications (e.g., CQE)Similar educational background, often with quality certifications
Work EnvironmentLeads quality initiatives across projects, often in senior or strategic rolesSupports quality assurance in specific projects or components
Industry UsageUsed in manufacturing, aerospace, automotive, and tech industriesCommonly used in similar industries for quality assurance roles
Search & ComparisonHigher-level strategic responsibilities, leadership in quality processesFocused on execution and support of quality standards

The main difference is that the Principal Design Quality Engineer holds a senior, strategic role overseeing quality across multiple projects, while the Design Quality Engineer focuses on supporting quality assurance within specific projects. Both roles require similar credentials but differ in scope and responsibility.

What cities are hiring for Principal Design Quality Engineer jobs?

Cities with the most Principal Design Quality Engineer job openings:

What states have the most Principal Design Quality Engineer jobs?

States with the most job openings for Principal Design Quality Engineer jobs include:

What are popular job titles related to Principal Design Quality Engineer jobs?

For Principal Design Quality Engineer jobs, the most frequently searched job titles are:

Infographic showing various Principal Design Quality Engineer job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 88% Physical, 1% Hybrid, and 11% Remote job distribution, with an average salary of $125,478 per year, or $60.3 per hour.

Principal Design Quality Assurance Engineer - Electrophysiology

Arden Hills, MN • On-site

Boston Scientific
Medical Equipment and Supplies Manufacturing • 10K+ employees

Other

Posted 25 days ago


Boston Scientific rating

8.5

Company rating: 8.5 out of 10

Based on 120 frontline employees who took The Breakroom Quiz


Job description

Additional Location(s): N/ADiversity - Innovation - Caring - Global Collaboration - Winning Spirit - High PerformanceAt Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions.About the roleThe Principal Design Quality Assurance Engineer will bring their leadership to sustaining projects for our innovative Electrophysiology cardiovascular products portfolio. Furthermore, they will develop, establish, and maintain quality-engineering methodologies, systems, and practices which meet BSC, customer, and regulatory requirements.Work ModeAt Boston Scientific, we value collaboration and synergy. This hybrid role is based in Arden Hills, MN and requires being on-site at least three days per week.Relocation assistanceNo relocation assistance is available for this position at this time.Visa sponsorshipBoston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time.Your responsibilities include:Lead Quality function for product sustaining teams within the BSC Quality System for Medical Electrical Equipment (MEE) and single use device (SUD) as part of a core group of Design Quality Assurance (DQA) Engineers.Provide quality and compliance inputs to project teams for project decisions and deliverables (i.e. Design Change Analysis; Design Inputs, Design Outputs; Test Method Development and Validation; Design Reviews; Design Verification and Validation; Usability Testing; SW Validation; Process Validation; and Labeling).Provide quality and compliance inputs for post market product sustaining activities, such as design changes, Non-Conformance Reports (NCEP); Corrective and Preventive Actions (CAPA’s); Product Inquiry Report/Field Action Assessment (PIRs); Field Signals Evaluations and Field Actions. Create, maintain and/or support safety risk management processes, including Hazard Analysis, Fault Tree Analysis, Task and Use Error Analysis, Risk Management Plan, Risk Management Report, and DFMEA.Lead projects as a DQA SME and work with R&D Engineers to review Hardware/Software systems architecture(s) and identify possible failure modes/risk control opportunities for these complex systems.Responsible for collaborating within teams to identify and implement effective controls to support development or maintenance of products to meet internal and external requirements.Building quality into all aspects of work by maintaining compliance to all quality requirements.Support internal and external regulatory audits as required.Mentor and provide design related technical guidance within the design assurance team.Other duties as necessary or required by the organization.What we're looking for in you:Required QualificationsBachelor’s of Science in Biomedical, Electrical Engineering or equivalent.10 years of medical device engineering experience, with experience in Medical Electrical Equipment/Systems (MEE / MES).Applied knowledge in the design verification and validation of Capital Equipment, including hardware, software, firmware.Experienced in working in a regulated environment for example FDA, ISO standards, EUMDR, IEC 60601, EN ISO 14971, IEC 62304 and EN ISO 13485.Strong leadership, relationship building, and team building skills.Demonstrated ability to mentor and coach others in analysis and risk based decision-making processes to balance business and compliance needs.Strong communication and presentation skills.Strong applied knowledge of statistical concepts, tools, and methodologies.Travel approximately 5-10%.Requisition ID: 633302Minimum Salary: $ 102100Maximum Salary: $ 194000The anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) – see www.bscbenefitsconnect.com—will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role. Compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, among other relevant business or organizational needs. At BSC, it is not typical for an individual to be hired near the bottom or top of the anticipated salary range listed above.Compensation for non-exempt (hourly), non-sales roles may also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements).Compensation for exempt, non-sales roles may also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).For MA positions: It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability.Boston Scientific transforms lives through innovative medical technologies that improve the health of patients around the world. As a global medical technology leader for more than 45 years, we advance science for life by providing a broad range of high-performance solutions that address unmet patient needs and reduce the cost of healthcare. Our portfolio of devices and therapies helps physicians diagnose and treat complex cardiovascular, respiratory, digestive, oncological, neurological and urological diseases and conditions. Learn more at www.bostonscientific.com and follow us on LinkedIn.Boston Scientific Corporation has been and will continue to be an equal opportunity employer. To ensure full implementation of its equal employment policy, the Company will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class.Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status. Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment. Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements. As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company’s policies or protocols change with regard to COVID-19 vaccination.Among other requirements, Boston Scientific maintains specific prohibited substance test requirements for safety-sensitive positions. This role is deemed safety-sensitive and, as such, candidates will be subject to a prohibited substance test as a requirement. The goal of the prohibited substance testing is to increase workplace safety in compliance with the applicable law. #J-18808-Ljbffr

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About Boston Scientific

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As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen.

Industry

Medical equipment and supplies manufacturing, manufacturing and construction

Company size

10,000+ Employees

Headquarters location

Marlborough, MA, US

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