Philips
Process Quality Engineer
Process Quality Engineer (Contract)
Location: Best
Duration Assignment: 1 Year (with possibility of extension)
Contract: via a Randstad company
Hours/week: 40
Budget range: €3.836 - €5.115 per month
In this role, you will have the opportunity to: Make life better!
Responsible for driving CAPA activities from issue identification to closure, effectively project managing all CAPA activities, ensuring the quality of CAPA record content and representing CAPAs during audits and CAPA Review Board meetings
Support deployment of Philips corporate processes within the GLOBAL MR R&D organization and drive related improvement activities and alignment across the different MR R&D sites. All of this as part of Phlips’ initiatives to drive continuous improvements on patient safety and quality.
When you choose to work at Philips you’ll work on life-changing projects; and contribute to innovative health technologies and solutions that improve billions of lives around the world.
You will be responsible for:
Planning, coordination, and delivery one or more QMS projects/programs and deploy across R&D organization.
Secure commitment from different stakeholders to deliver according to plan.
Build a project/program team from different capabilities and functional areas.
Ensure smooth deployment of processes and IT solutions across R&D organization.
Report status regularly to the leadership team.
Support the QMS Team on continuous updates of the QMS to reflect the changing needs of the business.
Support Team Members to make the most effective use of their contributions to the QMS.
Act as CAPA owner/facilitator/program manager.
To succeed in this role, you’ll need a customer-first attitude and the following:
Master’s or bachelor’s degree in technical profession.
7+ years of experience in high tech R&D domain of highly regulated businesses, with a proven track record in driving/leading process transformation deployments and tool deployments.
Good understanding of the hardware/software development lifecycle and related Quality Management Systems.
Process oriented with good knowledge of FDA and/or ISO regulations.
Excellent organizational skills to drive change and manage stakeholders.
Ability to cope with dynamics and complexity.
Proactive and able to act on own initiative.
Ability to train, coach and motivate people.
You are a part of:
The global System Integration & Verification (SIV) department of the MR-OEM R&D organization. Located in Best (Netherlands) you will work closely together with your peers in the MR Business and peers in other sites and businesses.
At Philips:
There are three core ways that define our ways of working: embracing flexibility, being at our best and impactful collaboration. We believe this enables us to deliver an outstanding experience to our customers and create the best place to work for people who share our passion.
We know just how important direct interactions are and work is more engaging when we are more frequently face-to-face, and that we experience better collaboration, which drives innovation. While we have many different types of roles across Philips most require a combination of in-person collaboration with colleagues and partners, usually at a Philips location, and individual focus time, which can be done remotely.
In return, we offer you:
For this project, you’ll work for Philips and become a contract or permanent employee of a Randstad company. As a contractor at Philips you'll enjoy cutting-edge challenges and unexpected experiences that make you a more in-demand professional.
Why work on a project at Philips?
If you’re looking for meaningful work and a chance to tackle complex challenges, broaden your skills and expertise and become an even more sought after professional, you’ll find all that and more with project work at Philips.
The Randstad companies are responsible for finding talent to provide services at Philips. If you are selected to provide services for Philips, you will be employed by Randstad and will not be an employee of Philips.