Job Title

Service Parts Quality Engineer

Job Description

Quality Group Circular Lifetime Solutions (CLS) oversees the Quality Assurance in the processes related to the supply and distribution (forward and reverse) of service parts, refurbished systems (CE), repair, services and their supply chain, including compliance with regulatory requirements and procedures for regulated products/businesses. We lead and coordinate the Quality support within the scope of service parts and repair to ensure successful and compliant processes with service parts, refurbished systems and repair business partners.

The role is about to assure that Quality systems of suppliers and Philips Health Systems meet Purchasing Controls and regulatory requirements.

Your role:

Support the quality teams to ensure adequate plans are in place for spare parts supply, and repair service providers, refurbished systems and 3rd party related activities
Collaborate with Supply Chain leaders to ensure all quality related processes and support where necessary to ensure successful supplier base to the regions
Monitor operational compliance of supply chain and repair for service and parts, reporting on a regular base and escalate in case compliance issues
Leads assigned areas in support of Products Transfers – process validations – planning
Supports assigned areas in service transfers
Supports the development and execution of operations quality disciplines such as Validations, Process Controls, Inspection Plans, Control Plans
Ensure raw materials/components/products and services are released from suppliers to Philips according to the agreed requirements.
Drive quality, compliance and continuous improvement at suppliers
Ability to travel as needed (15-25% per year)

You're the right fit if:

You have a Bachelor Degree in relevant technical function
You have a relevant experience in root cause analysis, corrective and preventive action methods
You are experienced in Product/process development and/or supplier quality improvement
You have knowledge about problem solving with quality tools such as: 6-sigma / 8-D / CAPA / FMEA/ 5WHY etc.
Exposure to production/quality development and control methods; CtQ definition, DfSS, SPC, APQP, FMEA, Control Plans, etc.
You have an auditing skill sets
You have an ability to write procedures and technical documentations
You have an excellent MS office skills
You are self-starter, curious
You are fluent in English

How we work togetherWe believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week.About PhilipsWe 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.• Learn more about our business.• 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.

#LI-Hybrid

#LI-EU

#GBS