×
Register Here to Apply for Jobs or Post Jobs. X

Medical Product Quality & Reliability Engineer

Job in Wilmington, Middlesex County, Massachusetts, 01887, USA
Listing for: Analog Devices
Full Time position
Listed on 2026-01-12
Job specializations:
  • Engineering
    Systems Engineer, Quality Engineering
Salary/Wage Range or Industry Benchmark: 100000 - 125000 USD Yearly USD 100000.00 125000.00 YEAR
Job Description & How to Apply Below
Position: Staff Medical Product Quality & Reliability Engineer

Staff Medical Product Quality & Reliability Engineer

6 days ago Be among the first 25 applicants

About Analog Devices

Analog Devices, Inc. (NASDAQ: ADI) is a global semiconductor leader that bridges the physical and digital worlds to enable breakthroughs at the Intelligent Edge. ADI combines analog, digital, and software technologies into solutions that help drive advancements in digitized factories, mobility, and digital healthcare, combat climate change, and reliably connect humans and the world. With revenue of more than $9 billion in FY24 and approximately 24 000 people globally, ADI ensures today's innovators stay Ahead of What’s Possible™.

Learn more at  and on Linked In and Twitter (X).

Job Summary

The Staff Medical Product Quality and Reliability Engineer provides strategic leadership in developing, implementing, and continuously improving verification, validation (V&V), and reliability strategies for medical devices. This role ensures compliance with global regulatory requirements, drives V&V maturity, and integrates reliability engineering throughout the product lifecycle. The Staff Engineer leads cross‑functional initiatives, mentors peers, and influences quality culture and regulatory readiness globally.

Key Responsibilities
  • Develop and implement comprehensive V&V and reliability strategies for new and existing medical devices.
  • Define and monitor V&V and reliability KPIs (e.g., MTBF, defect escape rates) to ensure performance targets are met.
  • Provide technical leadership for regulatory submissions (FDA 510(k), PMA, EU MDR) and global compliance.
  • Collaborate with R&D, Quality, Manufacturing, and Regulatory teams to define product V&V and reliability plans.
  • Conduct advanced reliability analyses (FMEA, Weibull, life data analysis, accelerated life testing, reliability growth modeling).
  • Develop and validate test methods for V&V and reliability, including automated and model‑based approaches.
  • Support Design for Reliability (DfR) initiatives and integrate predictive analytics for reliability trends.
  • Ensure adherence to global standards (ISO 13485, FDA QSR, ISO 14971, EU MDR, IEC 62304 for software).
  • Lead internal and external audits (FDA, Notified Body) and drive audit readiness and response activities.
  • Oversee post‑market surveillance and integrate reliability monitoring into CAPA processes.
  • Partner with suppliers to ensure component and system‑level V&V and reliability requirements.
  • Mentor engineers and cross‑functional teams on quality principles, regulatory expectations, and continuous improvement.
  • Influence change management and foster a culture of quality and reliability excellence.
Required

Skills and Qualifications
  • Bachelor’s degree in Engineering, Life Sciences, or related field (Master’s preferred).
  • 5+ years of experience in V&V and reliability within the medical device industry.
  • Expert knowledge of global regulatory requirements (FDA QSR, ISO 13485, ISO 14971, EU MDR, IEC 62304).
  • Strong proficiency in reliability tools, statistical methods, and quality systems (Six Sigma, eQMS).
  • Demonstrated success in leading audits and regulatory inspections.
  • Experience with risk management, post‑market surveillance, and CAPA integration.
  • Experience with digital tools for simulation, model‑based systems engineering, and automated test systems.
  • Exceptional communication, leadership, and cross‑functional collaboration skills.
  • Certifications:

    Lean/Six Sigma highly desirable; ASQ CRE preferred.

For positions requiring access to technical data, Analog Devices, Inc. may have to obtain export licensing approval from the U.S. Department of Commerce – Bureau of Industry and Security and/or the U.S. Department of State – Directorate of Defense Trade Controls. As such, applicants for this position – except US Citizens, US Permanent Residents, and protected individuals as defined by 8 U.S.C. 1324b(a)(3) – may have to go through an export licensing review process.

Analog Devices is an equal opportunity employer. We foster a culture where everyone has an opportunity to succeed regardless of their race, color, religion, age, ancestry, national origin, social or ethnic origin, sex, sexual orientation, gender, gender identity,…

To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)

Job Posting Language
Employment Category
Education (minimum level)
Filters
Education Level
Experience Level (years)
Posted in last:
Salary