Job Information
Philips Procurement Supplier Engineer BP MR in Best, Netherlands
As a Procurement Supplier Engineer you will be responsible for developing and managing suppliers capable of consistently supplying high-quality parts to Medical Device standards. You will 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 a great deal of learning from vide variety of manufacturing processes, supplier companies and their operations, Quality Management System of a medical device industry, supplier development and management involving APQP 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 assessment of suppliers and learning in great depth about Philips products and business.
In this role you will
Define project plan for all parts per supplier 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, Pune) involved parts impacted.
Assess design impact by reviewing SRPQP and accordingly work on design & development activities (CTQ/CTS, DMR & V&V) jointly with R&D, DQA and PIE teams.
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.
Location: our office in Best
Application Deadline: April 19th 2025
How to apply: As this role involves international collaboration, please send your application in English (CV and cover letter).
Offer includes: Competitive salary, performance bonus, allowances, discounts for our products and local benefits.
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 automotive, 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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