Senior Design Quality Engineer

Posted 11 Days Ago
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Murrysville, PA, USA
In-Office
92K-146K Annually
Senior level
Healthtech • Telehealth
The Role
Accountable for design quality and risk management across product lifecycle for sleep and respiratory medical devices. Create and oversee quality plans, validate design inputs, oversee design V&V, design transfer, and post-market performance. Perform technical assessments, post-market analytics, and initiate CAPA/field actions. Drive continuous improvement using PMS data and ensure compliance with regulatory and quality standards.
Summary Generated by Built In
Job TitleSenior Design Quality Engineer

Job Description

The Senior Design Quality Engineer is accountable for system/hardware design quality and risk management throughout the product life cycle for Philips Sleep & Respiratory Care products.  

Your role:

  • Ensures that appropriate quality plans are made that include all stages of the life cycle of the product and supports Quality Plan design
  • Provides independent oversight of the design input 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
  • Provides effective oversight of the execution of the Quality Plan, any Risk Management activities, and of all design related activities during the product/system lifecycle
  • Performs independent technical assessment on product quality performance and post-market product quality analysis. Provides analytics to the Business on the efficacy and efficiency of the design and product realization processes.
  • 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 5+ years’ experience in FDA regulated medical device environments, with a focus on Design Assurance/Control and strong Understanding of ISO 13485 / 9001 / FDA / Canada
  • 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 Murrysville, PA is $92,000 to $146,000.

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 Murrysville, PA.
  • May require travel up to 10%.

#LI-PH1

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 5+ years experience in FDA-regulated medical device environments with Design Assurance/Control
  • Strong understanding of ISO 13485, ISO 9001, FDA requirements and Canadian regulations
  • Proven experience in Risk Management (ISO 14971), FMEA/DFMEA, Design Verification and Validation
  • Experience with Root Cause Analysis, Defect Management, CAPA and post-market surveillance analytics
  • Detailed experience supporting processes and design quality tools for defect tracking, design traceability, and Design for Reliability
  • Bachelor's Degree in Quality, Engineering, or similar discipline
  • Must be able to meet physical, cognitive and environmental job requirements with or without accommodation
  • US work authorization required; employer will not sponsor visas
  • Must reside in or within commuting distance to Murrysville, PA; onsite office role (3+ days/week)

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
Alpharetta, GA
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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