Max. € 100,000/€ 100
Project & Program Management, Supply Chain
Detachering via YER, Interim / ZZP
Medical & Health, Manufacturing
Over deze vacature
Two periods assignment, from now-September 2018 and October - September 2019:
- Now-September 2018: Feasibility study
- October - September 2019: Deployment/implementation
The first period of the assignment is a feasibility study based on the new Medical Device Regulation (MDR) in de European Union. This MDR is implemented to protect civilians against non-correct working devices. The import of these devices needs to be compliant to EU guidelines and to the new MDR. In this first period, you will be analysing the process and the compliancy rules for Philips. After the feasibility study there should be an advice to continue or not continue with the current system and processes. Based on this advice the second stage of the assignment can continue (implementation of the research).
With a growing presence in cardiology, oncology, and women's health, Philips operates in the areas of Imaging Systems, Patient Care & Clinical Informatics, Home Healthcare and Customer Services. Philips combines its clinical expertise and human insights to create innovative solutions across the continuum of care, in partnership with clinicians and our customers, to provide better value and expand access to care for millions. Our teams are working hard every day to improve patient outcomes all the way from disease prevention and screening to diagnosis, treatment, therapy monitoring, and disease management. Irrespective of whether the care cycle takes the patient from doctor's office to hospital or hospital to home, or simply from one medical department to another, Philips Healthcare's unique medical solutions are designed to optimize the quality and flow of patient information and clinical decision making.
This role can be done by a freelancer of you will be employed by YER and seconded to Philips. We offer:
- Academic background
- Extensive experience in project management
- SAP GTS
- Knowledge of FDA or EU MDR
- Supply chain knowledge