17 Jan

Supplier Quality Engineer Vacature bij Philips Best

Functietitel
Supplier Quality Engineer
Bedrijf
Philips
Locatie
Best Nusa Tenggara Barat
Openingsdatum
17 Jan, 2018 30+ days ago

Philips Best met spoed nodig onderstaande werk positie als de Supplier Quality Engineer. Lees deze personeelsadvertentie zorgvuldig alvorens het aanbrengen van. Er zijn enkele kwalificaties, ervaringen en vaardigheden eisen dat de werkgevers nodig hebben. Doet je carrière geschiedenis passen deze eisen? Ervoor begrijpen dat u de rol die je solliciteert en dat zorg ervoor dat het geschikt is met uw vaardigheden en kwalificaties te.

Volg de online aanwijzingen, vul alle benodigde velden, en alle relevante informatie, zodat uw aanvraag correct is ingediend. Wanneer u klikt op 'Apply This Job' knop (opent in nieuw venster) wordt u meegenomen naar het online sollicitatieformulier. Hier wordt u gevraagd om persoonlijke en contactgegevens te verstrekken, reageren op werkgerelateerde vragen, en laten zien hoe u voldoet aan de belangrijkste selectiecriteria.

Supplier Quality Engineer Vacature bij Philips Best Vacatures Detail:

Your challenge

As a Supplier Quality Engineer you assure that Quality systems of suppliers and Philips Health Systems meet Purchasing Controls regulatory requirements. The scope of activities includes all QMS relevant. Purchasing Controls processes, systems and procedures, as well as Q&R processes indirectly related to Purchasing Controls (e.g., CAPA, audit). The suppliers in scope include Quality-relevant suppliers of specified components, spare parts, assemblies, contract manufactured and OEM manufactured devices, and software, services, logistics provider’s third-party manufacturers (TPMs) and consultants. You will participate in the development of suppliers’ Quality Assurance processes to ensure high quality and compliance in all markets that Philips Health Solutions serves. The Supplier Quality Engineer is accountable and responsible for supplier audits, agency inspections of Purchasing, and training.

Your responsibilities

Key Areas of Responsibility:
Identify key responsibilities in rough order of importance. Focus on the results that are expected from the job. For each statement, please set out the target in specific area or scope, the expected final results.
Set Quality system requirements to suppliers, including those for services, indirect quality relevant purchases (non-BOM), and QS requirements for suppliers in global markets.
Perform Qualification of suppliers to medical device standards and oversee their placement on the Approved Supplier List (ASL), including audit of Supplier Master File; Project book oversight as assigned
Conduct and oversee supplier audits- qualification and re-qualification, including finding closure
Collect, trend and report supplier quality metrics
Improve/develop quality systems at selected suppliers for QMS and compliance improvement
Develop purchasing controls processes and procedures, including those for BOM, non-BOM, services, spare parts and Markets
Evaluate and improve the effectiveness of purchasing controls and supplier quality processes and procedures, including Quality Agreements
Assist BG/Market in preparing for and defending Purchasing Controls in inspections by external agencies or internal Philips audits of Purchasing Controls processes
Manage and oversee BG Purchasing controls CAPA, including root cause identification, and effective and timely closure
Develop and deliver training to internal teams and suppliers on Philips Purchasing controls processes and procedures
Support as a Subject matter expert the Supplier Quality related processes towards projects (internal/ external projects). Risk management, purchasing controls.
Service Part Qualifications (PPA, APQP, PSW)
Your team

You will be a part of the Quality and Regulatory organization which is a structure of the Single Value added layer within Philips. In your role you support the Service Part Supply chain organization which is a member of the Global Customer service organization. The Supplier Quality team consists of 10 team members, based in the US, the Netherlands and China.

Our offer

We welcome you to a challenging, innovative environment with great opportunities for you to explore.

Our benefits are very competitive and designed around your preferences:

We offer a market conform salary
25 Days of leave and the possibility to purchase up to 20 extra days off annually
A variable bonus based on both Philips results and personal performance
Extensive set of tools to drive your career, such as a personal development budget, free training and coaching
Solid company pension scheme and attractive collective health insurance package
Opportunity to buy Philips shares and products with discount
Healthy work-life balance
We are looking for

To succeed in this role, you should have the following skills and experience

Bachelor or Master degree in technical field;
Knowledge of medical device regulations, e.g., ISO 13485, FDA cGMP, MDD, other global equivalent
Requires a minimum of 3 years of related work experience in highly regulated environment.
Experience in Product/process development and/or supplier quality improvement;
Experience in root cause analysis, corrective and preventive action methods and quality tools 6-sigma / 8-D / CAPA / FMEA/ 5WHY etc.
Auditing skillsets, up to and including certified SQ lead auditor training; with advanced manufacturing and/or special process auditing skills e.g., PCBA,
Ability to read and understand engineering drawing notation, tolerances, specifications
Experience with Software Databases, and excellence MS office skills (Word, Acces, Excel)
Contact

If you forgot your password, you can click the Forgot Password button on the Sign In screen to reset it. In case of technical difficulties, please send an email to careersite@philips.com .
(Note: To ensure fairness and legal compliance in our recruitment processes, only technical issues will be monitored through the above inbox. Please do not submit resumes or applications to this email, as they will not be reviewed. Only applications received through the online application process will be considered.)


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