As a Senior Quality Engineer, you will play a pivotal role in overseeing, leading, and guiding quality and risk management processes throughout the product life cycle within the organization Oral Healthcare which offers a range of oral care products, from electric toothbrushes, interdental cleaning, to whitening treatments. You also have the opportunity to support other product value streams such as interdental or whitening products on the top of power tooth brushes.
In this role you will be at the forefront of ensuring all design requirements are met and lead and provide analytics to the Business on the efficacy and efficiency of the design and product realization processes. In this role you will also mentor and train junior people within the team.
Your role:
Ensures and provides guidance that appropriate quality plans are made that include all stages of the lifecycle of the product and supports Quality plan design
Validates and provides guidance on key design inputs like: usability, reliability, performance, supportability, manufacturability, localizability, safety, security, privacy, serviceability, sustainability and costs
Leads and 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 on multiple product ranges
Leads and provides guidance 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
Act as a point of contact for multiple projects responsible to ensure that hardware design meets quality and compliance standards for every milestone
Executes and provides guidance on risk management activities, biocompatibility testing, product failure rate and reliability estimations.
Mentor and train other team members on quality related projects or issues.
You're the right fit if:
Possess 6+ years of Quality Engineering experience in a regulated environment, preferably within the Medical Device or Pharmaceutical industry.
Hold a Bachelor’s degree in a scientific discipline, with a preference for Engineering.
Demonstrated ability to independently produce and guide others in completing Quality Engineering Documents, as well as experience with Quality Data Analysis.
Proven records in managing complexity of products or systems in multi-disciplinary setting, preferably NPI (New Product Introduction) projects
Certification in Quality Engineering or Quality Reliability Engineering would be preferred.
How we work together
We believe that we are better together than apart. For this role 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.
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• 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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