Design Quality Engineer

3 Minutes ago • 8 Years +

Job Summary

Job Description

The Design Quality Engineer (DQE) oversees the design input process, design Verification & Validation (V&V) activities, design transfer, and product performance to ensure design requirements are met. This role involves creating quality plans, validating design inputs (usability, reliability, performance, etc.), providing oversight of the Quality Plan, Risk Management activities, and design-related activities throughout the product lifecycle. The DQE performs technical assessments, leads problem-solving, analyzes post-market data, and ensures Quality Management System compliance. Responsibilities include planning, controlling, and assuring product and process quality, ensuring compliance during design reviews, and facilitating Design for Quality & Reliability best practices.
Must have:
  • Engineering degree with 8+ years industry experience.
  • Expertise in Design Quality or Reliability Engineering.
  • Mandatory medical device industry experience.
  • Ability to define systems quality and reliability plans.
  • Ability to contribute to Risk Management and lead FMEA activities.
  • Strong exposure to Design Controls.
  • Ability to lead reliability analysis and assess design risks.
  • Experience in reviewing DHF and DMR documents.
  • Understanding of global medical device regulations and standards.

Job Details

Job Title

Design Quality Engineer

Job Description

Job title:
Design Quality Engineer - Medical Devices

The Design Quality Engineer DQE 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. The DQE also provides analytics to the Business on the efficacy and efficiency of the design and product realization processes
Your role:

  • Ensure appropriate quality plans are made that include all stages of the life cycle of the product and supports Quality Plan design.
  • Validate key design inputs like usability, reliability, performance, supportability, manufacturability, localizability, safety, security, privacy, serviceability, sustainability, and costs.
  • Provide effective oversight of the execution of the Quality Plan, any Risk Management activities, and of all design related activities during the product/system lifecycle.
  • Perform independent technical assessment on product quality performance and post market product quality analysis.
  • Can Lead quality related problem solving and root cause analysis during design and manufacturing.
  • Uses post-market analytics and statistics to report on product quality performance in the field (provide feedback to manufacturing, suppliers or design teams) and initiates field actions when required.
  • Performs independent technical assessment on product quality performance and post market product quality analysis.
  • Provide leadership and oversight to ensure Quality Management System Compliance.
  • Be able to plan, control, and assure product and process quality in accordance with quality principles, which include planning processes, material control, acceptance sampling, and measurement systems.
  • Ensure the compliance requirements are met during Design review , design verification & Design validation , Design transfer.
  • Apply and facilitate Design for Quality & Reliability best practices (FMEAs, robust design, V&V, root cause analysis & problem solving).


You're the right fit if: (4 x bullets max)

  • An Engineering degree in any discipline with at least 8+ years of relevant industry experience.  Core expertise in Design Quality, Systems Engineering, or Reliability Engineering.
  • Medical device industry experience is mandatory .
  • Ability to define detailed systems quality and reliability plans for new medical product developments to ensure those are safe, effective and reliable.
  • Ability to contribute to Risk Management and lead FMEA activities for new products and assurance that control measures are translated in appropriate critical requirements.
  • Strong exposure to application of Design Controls; ability to do thorough Design Reviews during new product development to ensure robust designs that further improve patient safety and product quality.
  • Ability to partner with V&V teams to assure thorough Verification, Validation and Usability testing.
  • Ability to lead reliability analysis to assess the risks associated with design concepts.
  • Experience with adequate and accurate review of DHF and DMR documents.
  • Understanding of global medical device regulations, requirements, and standards, such as 21CFR820, ISO13485, EU MDR, , and ISO 14971.
  • Experience with working in multidisciplinary teams in a high-tech R&D environment.
  • You continuously strive for excellence as a way of life and can inspire others to adopt this mentality of prioritizing quality above all else.
  • You are a self-starter who embraces the change

How we work together
We believe that we are better together than apart. 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.

Indicate if this role is an office/field/onsite 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 the lives of others.
• Learn more about our business.
• Discover our rich and exciting history.
• Learn more about our purpose.

If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our commitment to diversity and inclusion here.

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About The Company

Over the past decade we have transformed into a focused leader in health technology.

At Philips, our purpose is to improve people’s health and well-being through meaningful innovation. We aim to improve 2.5 billion lives per year by 2030, including 400 million in underserved communities.

We see healthcare as a connected whole. Helping people to live healthily and prevent disease. Giving clinicians the tools they need to make a precision diagnosis and deliver personalized treatment. Aiding the patient's recovery at home in the community. All supported by a seamless flow of data.

As a technology company, we – and our brand licensees – innovate for people with one consistent belief: there’s always a way to make life better.


Visit our website: http://www.philips.com/
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