Reliability Engineer

As a Reliability Engineer in the Sleep and Respiratory Care (SRC) R&D team at Philips, you will contribute to product development, focusing on advanced life support and data management solutions. Your responsibilities include performing reliability activities, executing testing, writing protocols and reports, contributing to risk analyses, and collaborating with cross-functional teams to ensure product reliability and assist in problem-solving.

Must Have

• Work collaboratively with senior reliability engineers to perform reliability activities on products.
• Work collaboratively with reliability technicians to execute reliability testing.
• Write test protocols and reports using Good Documentation Practices.
• Contribute to risk analyses (FMEAs, FTA, etc.).
• Perform reliability activities, including life analysis, block diagrams, reliability demonstration testing, ALT / HALT / HASS, durability testing, etc.
• Work cross-functionally with Design Quality, Systems Engineering, V&V, Hardware Design, and Software Design.
• Assist in problem identification, root cause analysis, corrective actions, and verification of the solution.
• Bachelor’s degree in Electrical/Electronics/Mechanical Engineering or related field.
• Minimum 3 years of experience in medical device or similar industry.
• Capable of critical thinking, troubleshooting, and problem solving.
• Familiarity with Microsoft Suite (Word, Excel, Outlook, Teams, PowerPoint).
• Familiarity with lab tools including soldering equipment, multimeters, and hand tools.
• Experience in an FDA regulated environment.
• Strong understanding of medical device industry regulatory requirements.
• Solid understanding of medical device product development.

Good to Have

• Master’s degree.
• Vocational Education such as statistics, engineering, 6Sigma.
• Familiarity with software tools (i.e. LabView, Arduino, ReliaSoft, Minitab).
• Certified Reliability Engineer (CRE).
• Six Sigma Green Belt.
• Design Control experience with Class III medical devices.
• Experience in designing and assessing compliance to national/international standards.

In this role, you have the opportunity to

Be an integral part of the Sleep and Respiratory Care (SRC) R&D team, actively participating in Sleep and Respiratory Care product development. SRC team has a broad product portfolio of advanced life support solutions and data management solutions. Our mission is to design, produce, and deliver every solution as if the life of someone we love depends on it. Every day, we empower and enable our customers – from clinicians to paramedics, first responders to the everyman – to save lives using our innovative, market-leading technology.

We are looking for a passionate Reliability Engineer to join us as we strengthen our product portfolio, expand our services and solutions, and bring game-changing technology to market. This team member will be responsible for working collaboratively with a team of cross-functional engineers.

You are responsible for

• Work collaboratively with senior reliability engineers to perform reliability activities on products.
• Work collaboratively with reliability technicians to execute reliability testing.
• Write test protocols and reports using Good Documentation Practices.
• Contribute to risk analyses (FMEAs, FTA, etc.)
• Perform reliability activities, including life analysis, block diagrams, reliability demonstration testing, ALT / HALT / HASS, durability testing, etc.
• Work cross-functionally with Design Quality, Systems Engineering, V&V, Hardware Design, and Software Design to perform necessary tasks.
• Assist in problem identification, root cause analysis, corrective actions, and verification of the solution

You're the right fit if:

• Bachelor’s degree in Electrical/Electronics/Mechanical Engineering or related field. Master’s degree is preferred.
• Total 7+ years’ experience with Minimum 3 years of experience in medical device or other similar industry with Vocational Education such us statistics, engineering, 6Sigma.
• Be hands-on and self-motivated.
• Excellent attitude and a collaborative spirit.
• Capable of critical thinking, troubleshooting, and problem solving.
• Familiarity with Microsoft Suite (Word, Excel, Outlook, Teams, PowerPoint)
• Familiarity with lab tools including soldering equipment, multimeters, and hand tools.
• Capability to excel in a high performing team environment and work with multiple projects simultaneously.
• Experience in an FDA regulated environment.
• Familiarity with software tools (i.e. LabView, Arduino, ReliaSoft, Minitab, etc.)
• Certified Reliability Engineer (CRE)
• Strong understanding of medical device industry regulatory requirements including ISO Standards (ISO 13485 and ISO 14971), EUMDR, IEC 62304, IEC 60601, IEC 62366.
• Six Sigma Green Belt
• Develops and maintains effective relationships and is capable of quickly earning trust and respect.
• Proven ability to communicate in both verbal and written form to technical and non-technical customers, stakeholders, and various levels of management.
• Solid understanding of medical device product development, preferably Design Control experience with Class III medical devices. (FDA CFR Title 21, 820.30)
• Experience in designing and assessing compliance to national/international standards.

How we work together

We believe that we are better together than apart. This means working in-person at least 3 days per week.

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 culture of impact with care here.

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