Philips

QMS Manager

Posted Sep 6, 2024
Project ID: PHIAJP00000488
Location
Eindhoven
Hours/week
40 hrs/week
Timeline
1 year
Starts: Nov 1, 2024
Ends: Oct 31, 2025
Payrate range
4500 - 7000 €/hr
Application Deadline: Sep 17, 2024 12:00 PM

QMS Manager (Contract)

Location: High Tech Campus, Netherlands

Duration Assignment: 12 months (with possible extension)

Contract: via a Randstad company

Hours/week: 40

Budget range: €4,500 - €7,000 moths salary

In this role, you can challenge the QMS Manager position by driving the maintenance, enforcement, and continuous improvement of the Quality Management System (QMS) to ensure compliance with both medical and non-medical regulatory standards. You will play a pivotal role in ensuring product quality, from development to market launch and post-market surveillance.

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:

  • Maintaining and enforcing a compliant and effective QMS for Quality and Regulatory (Q&R) processes and product quality.

  • Collaborating with Quality Managers across the organization to complete and maintain the QMS, with a strong focus on product development, launch, and maintenance.

  • Managing internal and external audits to ensure ongoing QMS compliance and certification.

  • Coordinating QMS-related activities between Philips IP&S, Research, and other stakeholders.

  • Supporting internal processes such as Change Control, Corrective and Preventive Actions (CAPA), and training administration.

  • Ensuring compliance with regulatory requirements like FDA, EU-MDD/MDR, and CFDA for ongoing and new ventures.

  • Driving continuous improvement initiatives and tracking performance indicators related to QMS and regulatory compliance.

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

  • A Bachelor's or Master’s degree in Science or Quality Engineering.

  • 5-10 years of experience in a highly regulated industry, preferably medical devices.

  • Proven experience as a Quality Manager handling processes like regulatory submissions, post-market surveillance, and QMS setup.

  • Strong understanding of compliance and ethics in an innovative environment.

  • Experience with software-driven and AI-enabled solutions is highly preferred.

  • Excellent stakeholder management and communication skills in English.

  • A team-oriented approach with the ability to lead and elevate teams.


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.

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