Job Title
Supplier Quality Engineer - Magnetic Resonance
Job Description
As a Supplier Quality Engineer, you will be responsible for developing, releasing, and managing suppliers’ capability of consistently supplying high-quality parts to Medical Device standard by use of IQ, OQ, PQ and TMV principles. You will collaborate and team-up with cross-functional teams including R&D, Procurement, Manufacturing Engineering, Factory Operations, Operations Quality, Supply Chain teams amongst others to manage suppliers involved in new product development and sustaining production in Best and Latham. The role offers requires knowledge of a wide variety of manufacturing processes, supplier companies and their operations, Quality Management System of a medical device industry, supplier development and management involving APQP (according to IQ.OQ/PQ principles) and SCAR/correction actions. With an opportunity to travel up to 20% domestically and up to 5% internationally, the role will offer exposure for on-site assessments of suppliers and learning in great depth about Philips products and business.
In this role you will
* Complete IQ-OQ-PQ processes validation as per ISO13485, FDA21CFR guidelines through supplier on site assessment and qualification.
* Complete APQP activities including PSW, Statistical process controls, line readiness etc.
* Define a project plan for supplier products based on risks assessment and identified priority.
* Define remediation program scope for NPI and existing production parts.
* Evaluate implementation priority by assessing complaints, special processes & other key design parameters.
* Launch Process validation remediation program for MR Suppliers across regions (Best, Latham) together with the team in Pune.
* Assess design impact by reviewing supplier’s process controls based on Philips design package together with the supplier and accordingly work on design & development activities (CTQ/CTS, DMR & V&V) jointly with R&D, Design Quality and Process Industrilization teams.
* Connect, collaborate with the R&D team to secure Design for Excellence in relation to product design is securing an efficient design in relation to qualification.
You're the right fit if:
* You have at least a Bachelor of Science degree in Engineering or a related field.
* 5 + years of related work experience in aerospace, medical device or similarly regulated industry.
* Experience in APQP/PPAP component qualification methodology, specifically process validation IQ-OQ-PQ
* Experience in corrective and preventive action/ CAPA/ SCAR/ 8D tools for continuous improvement
* Experience in supplier management (supplier quality or supply chain or procurement functions)
* You’re able to collaborate with a wide range of stakeholders across the organization. Lead challenging situations and team up to drive winning solutions. Act urgently with both business and compliance in mind.
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.
This role is an office 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 improve the lives of others.
* Learn more about our business.
* Discover our rich and exciting history.
* Learn more about our purpose.
* Read more about our employee benefits.
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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