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Hold a pivotal position to disrupt Medtech and make a real difference for patients.
The FORS group is a dedicated corporate venturing organization tasked to create new solutions for IGT, focusing on procedure innovation and new business model development in the cardio-vascular domain.
FORS is a unique technology that enables real-time 3D visualization of the full shape of devices inside the body without the need for fluoroscopy thus allowing us to break through the current limitations of image guided therapy by reducing the dependency on fluoroscopy while vastly improving the visualization of intra-body devices.
More about FORS: www.Philips.com/FORS-technology
In this customer-centric, fast-learning and agile venture environment we value drive, creativity and solution oriented end-to-end business thinking, and we are looking to hire a Quality Engineer that will actively engage with the key people of the FORS team.
Here you will establish and operationally execute quality strategies, based on a deep understanding of the quality management system processes as well as normative and regulatory requirements.
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
Validates key design inputs like: 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 life cycle
Performs 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
Act as a single point of contact (person assigned to project team) responsible to ensure that hardware design meets quality and compliance standards for every milestone
You're the right fit if:
Rich experience in the field of design transfer and post-market quality assurance
Rick experience in the field of manufacturing of Class III, sterile, (implantable) in-body medical devices.
Rich experience in the field of document reviews, CAPA and improvement projects
Preferable experience in working in venture / start-up setups incl. basic business understanding
Preferable experience on reliability engineering
Preferable experience on guide wires & sterile products
Innovative mindset & entrepreneurial spirit, hands-on approach
Excellent analytical and conceptual skills and structured way of working
Passionate personality with outstanding communication and interpersonal skills
About Philips
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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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