Design Quality Engineer

Posted Yesterday
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Bedford, MA, USA
In-Office
103K-163K Annually
Mid level
Healthtech • Telehealth
The Role
Lead design quality and post-market complaint investigations for image-guided therapy products. Ensure design inputs/outputs, V&V, design transfer, risk management (ISO 14971), and design history files meet regulatory and quality standards. Perform post-market data analysis, initiate CAPA/field actions, and support continuous improvement across product lifecycle.
Summary Generated by Built In
Job TitleDesign Quality Engineer

Job Description

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

Your role:

  • Ensures that appropriate quality plans are followed with a focus on sustaining and product complaint investigations.
  • Provides input to design I/O process, design V&V activities, design transfer and product realization, and performance in the field to ensure that all design requirements are effectively met. 
  • Validates key design inputs: usability, reliability, performance, supportability, manufacturability, localizability, safety, security, privacy, serviceability, sustainability and costs
  • Maintain Desing history files updated.
  • Provides effective input for Risk Management activities, and of all design related activities during the product/system lifecycle
  • Perform routine risk management updates.
  • Performs technical assessment on product quality performance and post-market product quality analysis.
  • Performs post-market data analysis/statistics to report on product quality performance in the field and to the Business on the efficacy and efficiency of the design and product realization processes.  
  • Initiates field actions/CAPA when required.

You're the right fit if:

  • You have a minimum of 3+ years’ experience in FDA regulated medical device environments, with a focus on Design Assurance, Sustaining and Post Market Complaint investigations.
  • You have proven experience/knowledge in Risk Management (ISO 14971), FMEA/DFMEA, Design Verification/Validation, Root Cause analysis and Defect Management.
  • You have detailed experience in identifying, promoting, and supporting processes and design quality tools for use in tracking/preventing product defects, design traceability, and Design for Reliability.
  • You’re experienced in utilizing Post Market Surveillance (PMS) insights/data analytics to lead continuous improvement throughout all stages of the product lifecycle.
  • You’re able to share knowledge, insights regarding quality standards, and regulatory requirements.
  • You have a minimum of a Bachelor’s Degree (Required), in Quality, Engineering or similar disciplines.
  • You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this position. 

How we work together:

We believe that we are better together than a part. For our Office-based teams, this means working in-person at least 3 days per week. Onsite roles require full-time presence in the company’s facilities. Field roles are most effectively done outside of the company’s main facilities, generally at the customers’ or suppliers’ locations. This is an Office role.

About Philips:

We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality. healthcare that we all deserve. Do the work of your life to help improve the lives of others.

  • Learn more about our business.
  • Discover our rich and exciting history.
  • Learn more about our purpose.
  • Learn more about our culture.

Philips Transparency Details:

  • The pay range for this position in Bedford, MA is $103,000 to $163,000.

The actual base pay offered may vary within the posted ranges depending on multiple factors including job-related knowledge/skills, experience, business needs, geographical location, and internal equity.  

At Philips, it is not typical for an individual to be hired at or near the top end of the range for their role and compensation decisions are dependent upon the facts and circumstances of each case. 

In addition, other compensation, such as an annual incentive bonus, sales commission or long-term incentives may be offered.  Employees are eligible to participate in our comprehensive Philips Total Rewards benefits program, which includes a generous PTO, 401k (up to 7% match), HSA (with company contribution), stock purchase plan, education reimbursement and much more.  Details about our benefits can be found here. 

Additional Information:

  • US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa, now or in the future.
  • Company relocation benefits WILL NOT be provided for this position.  For this position, you must reside in or within commuting distance to Bedford, MA
  • May require travel up to 10%.

This requisition is expected to stay active for 45 days but may close earlier if a successful candidate is selected or business necessity dictates.  Interested candidates are encouraged to apply as soon as possible to ensure consideration.

Philips is an Equal Employment and Opportunity Employer including Disability/Vets and maintains a drug-free workplace.

Skills Required

  • Minimum 3+ years experience in FDA-regulated medical device environments focusing on Design Assurance, Sustaining, and Post Market Complaint investigations.
  • Proven experience/knowledge in Risk Management (ISO 14971), FMEA/DFMEA, Design Verification/Validation, Root Cause Analysis, and Defect Management.
  • Experience utilizing Post Market Surveillance (PMS) insights and data analytics to drive continuous improvement.
  • Bachelor's Degree in Quality, Engineering, or similar discipline.
  • Ability to maintain and update Design History Files and perform routine risk management updates.
  • Knowledge of quality standards and applicable regulatory requirements for medical devices.
  • US work authorization required; employer will not sponsor work visas.
  • Must reside in or within commuting distance to Bedford, MA and be able to work on-site at least 3 days per week.
  • Ability to perform required physical, cognitive, and environmental job functions with or without accommodation.

Philips Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Philips and has not been reviewed or approved by Philips.

  • Retirement Support Retirement support is positioned as a standout, including a strong 401(k) match (often described at 7%) alongside pensions in some contexts.
  • Flexible Benefits Flexible benefits are emphasized through choice in health insurance options and a broad “Total Rewards” approach that combines compensation, health and wellness, and work-life support.
  • Leave & Time Off Breadth Leave and time off breadth appears strong, with generous paid time off and policies covering parental leave, caregiving responsibilities, volunteering, and family medical leave.

Philips Insights

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The Company
HQ: Cambridge, MA
80,000 Employees
Year Founded: 1891

What We Do

Do the work of your life to help the lives of others. As a leading health technology company, it is our purpose to improve people’s health and well-being through meaningful innovation. Our goal is to improve 2.5 billion lives per year by 2030. ​ ​ We also strive to be the best place to work for people who share our passion, by promoting personal development, inclusion and diversity while acting responsibly towards our planet and society.

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