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Quality System BPE, Q&R

Philips International B.V.

9037530 | EINDHOVEN | Detachering | HBO | 40 uur | publicatiedatum 

Solliciteer

Over de functie

Your challenge
Part of the End 2 End program, the Quality System Business Process Expert supports the development, deployment and maintenance of the Quality Management System within Philips Healthcare, ensuring Philips cross sector harmonization, standardization and regulatory compliance.
You will ensure process compliance to regulations, and that optimization and efficiency are built into the Business Management and Quality Management System processes across all sectors and groups in partnership with the other business functions.

Location: Eindhoven, Netherlands with potential travel to Amsterdam, Netherlands

Your responsibilities
Provide compliance and Quality Management System process improvement support to the E2E Program teams to ensure compliance with optimization and efficiency in E2E processes.
 
Your main responsibilities are:

  • Quality Management System Business Process Expert, acting in support of the Philips Healthcare Quality Assurance team and Q&R Business Process Owner, across the Philips Q&R network for the E2E program
  • Participate directly as the Philips Healthcare Quality Management System Business Process Expert in Philips “Process Capabilities” deployment programs, in the Idea to Market (I2M), Market to Order (M2O), and/or Order to Cash (O2C) arenas. Ensuring compliance, efficiency and effectiveness of the processes within the Philips Healthcare sector, cross sectors, and at Philips corporate.
  • This entails a thorough knowledge, as example, of Design (I2M), Marketing & Brand & Promotions (M2O), Production & Servicing (O2C) and Procurement /Purchasing
  • Includes, but is not limited to all Idea to Market (I2M), Market to Order (M2O), and/or Order to Cash (O2C) processes.
  • Support cross-Philips setup and deployment of the Quality Management Systems along business model lines as identified by End to End teams through the creation of Quality Transition Plan(s) that identifies appropriate Q&R activities to ensure compliance.
  • Work with Philips End to End & ARIS process modeling teams, Business Management System and Quality Management System owners, as well as any other stakeholders to ensure new process descriptions and procedures (PDDs – Process Definition Documents) are efficient, effective, and compliant to the applicable regulations
  • Work with Philips Software validation teams to ensure fully integrated, validated and compliant Philips Integrated Landscape (PIL) software application are deployed.
 Your team
  • Quality Assurance is an integral aspect of the global healthcare business including device design, development, manufacture, distribution, worldwide device marketing, sales, service, and post-market surveillance. This position is intimately involved in the process of ensuring Quality System Regulations are embedded within business processes and supports the harmonization of identified key processes by which the company and its sectors operate
  •  

Functie-eisen

We are looking for

  • Bachelor’s degree, preferably in a scientific discipline
  • Minimum of 7 years of experience working in Quality Assurance / Quality Engineering / Quality Systems supporting multiple functional disciplines within a global medical device industry.
  • Proven experience in Quality Management System processes, including cross sector or business process standardization, ensuring effectiveness and efficiency while maintaining compliance with worldwide regulations
  • A comprehensive understanding of the diverse worldwide medical device quality regulations, including areas of device design, development, manufacture, distribution, worldwide device marketing, sales, service, and post-market surveillance
  • An ability to successfully communicate and educate Quality Management System regulations, policies and strategies to teams at all levels of the organization
  • Experience with deployment of Quality Management System processes as identified
  • This position requires, and. Extensive knowledge of FDA QSR’s, ISO 13485, JPAL, China GMP’s and other worldwide Quality System Regulations.

Arbeidsvoorwaarden

Arbeidsvoorwaarden
Yacht is a contractor for highly educated professionals (BSc, MSc, or PhD) who’ll work on site and innovate together with our customers to find smart solutions. Being part of the world wide Randstad Group we have an extensive network of clients and professionals.

 

Bedrijfsinformatie

Bedrijfsinformatie

Working as a high tech professional within Yacht means you will work on interesting and challenging long term projects for our clients in the Dutch “Brainport” Eindhoven region, mainly on projects at our clients’ Research & Development departments. Our Brainport region is considered to be the smartest region in the world! We cooperate with high tech companies that work on the cutting edge of technology. To give you an example of our portfolio: ASML, Philips Healthcare, Philips Lighting, Philips Research, TNO, FEI company, DAF, VDL ETG, Océ and many others.
 
 

Contactinformatie

Voor meer informatie neem je contact op met Bram Geerets via telefoonnummer 06-55724609

Werken voor Yacht
Yacht is dé organisatie van en voor professionals. Wij verbinden professionals en organisaties die het verschil willen maken. Ons doel is optimaal resultaat: jou als professional uitdagend werk bieden waarmee jij de organisaties van onze opdrachtgevers blijvend verbetert. Behoor jij tot de beste professionals in jouw vak? Wil je samen met vakgenoten het verschil maken bij toonaangevende organisaties? Dan willen we jou graag leren kennen.

Solliciteer

Uiteraard staat deze vacature open voor zowel mannen als vrouwen.