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Philips QMS Director 
Germany, Hesse 
868616356

19.11.2024

Your role:

  • Ensure our Quality Management Systems (QMS) remain effective and compliant.

  • Lead and inspire QMS and CAPA teams, along with Program Management.

  • Take charge of transforming our current QMS into a unified PQMS structure.

  • Orchestrate our QMS architectural design, including proposing changes to central compliance teams.

  • Manage and streamline all QMS processes, keeping them FDA-ready.

  • Oversee local and global Quality and Regulatory processes, ensuring they meet all requirements. And owning the PQMS governance.

  • Drive continuous improvement initiatives in the MRI Business Unit.

  • Manage all relevant areas of QMS, including but not limited to management review, document control, audits, etc

You're the right fit if:

  • A Master university degree with a minimum of 10 years working experience in similar fields of expertiseor 12 years experience with bachelor degree.

  • Experienced in diverse medical device companies and with internal / external audits and managing organizations certified under ISO9001, ISO13485 and FDA regulated.Including front room experience hosting FDA inspections.

  • Strong strategic thinking and a proven track record ofglobaltransformational and continuous improvement success in combination withgreatstakeholder management skills.

  • Strong people management skills to lead and motivate diverse teams inmultiplelocations effectively.

  • Excellent communication and persuasive abilities.


This role is an office role.
We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others.
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