Staff Design Quality Engineer

undefined ago • 3 Years + • Quality Assurance

Job Summary

Job Description

The Quality Engineer is accountable for oversight of system and hardware quality and risk management throughout the product life cycle. This role provides independent oversight of the design input process, design V&V activities, design transfer and product realization, and performance in the field to ensure all design requirements are met. The engineer also provides analytics to the Business on the efficacy and efficiency of design and product realization processes.
Must have:
  • Provide Sustaining Design Assurance Quality Engineering support to sustaining (MLD) projects.
  • Provide support to teams in resolving issues and technical challenges for commercialized products.
  • Create Issue Impact Assessments (IIA's) to analyze and document risk assessment.
  • Ensure that teams pro-actively incorporate effective QMS compliance planning.
  • Ensure that all required Risk Management processes and activities are followed.
  • Provide support to CAPA's, complaint analysis and trending, Design and Technical reviews.

Job Details

Sustaining Design Quality Engineer

The Quality Engineer is accountable for oversight of system and hardware quality and risk management throughout the product life cycle. 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. Give analytics to the Business on the efficacy and efficiency of the design and product realization processes

Your role:

  • Provide Sustaining Design Assurance Quality Engineering support to sustaining (MLD) projects including design changes, supplier changes, process changes, etc. while embracing and upholding Patient Safety and Quality as highest priority.
  • Provide support to teams in resolving issues and technical challenges for commercialized products - including field issues, manufacturing issues, supply-chain-driven issues, etc. Support investigations and data analysis.
  • Create Issue Impact Assessments (IIA's) to analyze and document risk assessment per established procedures and with cross-functional team input.
  • Ensure that teams pro-actively incorporate effective QMS compliance planning within their project plans. Work with teams to ensure that applicable activities are planned, executed, and documented in an efficient, QMS compliant manner.
  • Ensure that all required Risk Management processes and activities are followed and appropriately documented.
  • Provide support to CAPA's, complaint analysis and trending, Design and Technical reviews, etc. as assigned.

You're the right fit if:

  • You have a Bachelor’s degree in biomedical engineering, mechanical or electrical engineering, or related technical degree with 3+ years of experience;
  • OR bachelor’s degree with 3+ years of experience in a medical device or regulated industry.
  • You have experience with CAPA process, risk assessments, as well as global medical device regulations, requirements, and standards such as 21 CFR Parts 820, 803, 806, and ISO13485, ISO 14971, and ISO9001.

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

At Philips, we believe that every human matters. As a global health-tech leader, we focus on improving people’s health and wellbeing through meaningful innovation. The people who work here share our passion and are motivated to bring this purpose to life.For more than 130 years, we have been creating technologies and innovations that improve people's lives and support healthcare practitioners. Headquartered in the Netherlands and operating in more than 100 countries globally, we focus our advanced technology and deep clinical and consumer insights on Precision Diagnosis, Image Guided Therapy, Enterprise Informatics, Monitoring/ Connected Care, Sleep & Respiratory Care and Personal Health.Together, we deliver better care for more people because we believe that every human matters.

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