Philips Supplier Quality Manager 

Germany, Hesse 

288287072

Supplier Quality Manager

You are responsible for ASL (Approved Supplier List) Management and Supplier Audit planning and execution to ensure compliance with Philips processes and regulations. You must work very closely with R&D, Operations and Procurement from the factory in Best/NL. Therefore, your working location is Best/NL. You ensure compliance with the Supplier Quality and Purchasing controls requirements.

Your role:

• Planning and execution of Supplier Audits according Audit plan and managing follow up activities like SCARs (Supplier Corrective Action Requests).

• Approved Supplier List (ASL) Management and ensures compliance with required supplier records.

• Gives input to purchasing control processes, procedures & systems in compliance with applicable regulations.

• Sets/updates purchasing control requirements to suppliers, classification of suppliers, and risk categorization.

• Participates / supports integration and validation of purchasing procedures with supporting IT and data applications for effective operationalization.

• Owns the full process of supplier qualification, audit, and assessment.

• Participates in supplier selection process; maintains the Approved Supplier List (ASL) and documented evidence of evaluation records.

• Provides regular feedback to the Business Process Owner (BPO) team for further process improvements.

• Supports internal and external Audits in terms of ASL & Supplier Audits.

You're the right fit if:

• You have a working knowledge of medical device regulations, e.g., ISO 13485, FDA cGMP, MDR, another global equivalent.

• Minimum of 5 years of related work experience in Supplier Quality.

• You are a certified Auditor.

• Min. Bachelor’s degree in an Engineering discipline.

• Experience in Manufacturing Processes and familiarity with Advanced Product Quality Planning (APQP) process.

• Experience in problem solving with quality tools such as: 6-sigma / 8-D / CAPA / FMEA/ 5WHY etc.

• Excellent knowledge of production/quality development and control methods; CtQ definition, DfSS, SPC, APQP, FMEA, Control Plans, etc.).

• You’ve got a solid technical background (you understand engineering drawing notation, tolerance, specifications).

• You’re able to prioritize and work in a structured manner.

• Good Team player with good communication skills.

• Fluently English and Dutch is a plus.

• Travelling 20%, mainly in Europe.

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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