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QC Engineering Manager

Excellent opportunity for a QC Engineering Manager to join an innovative start up Medical Devices company based in Belgium. The role will be reporting to the VP of Quality and Regulatory. This role will focus on improving quality of operational processes and be responsible for the design and implementation of verification & validation plans & protocols to effectively measure and assess the quality and performance of its in-process and finished devices.

Overview of your responsibilities (full job description available on request):

  • Oversee inspection & testing of products to confirm Quality performance`
  • Develop and approve V&V and test method validation protocols and reports
  • Foster a quality culture to ensure quality in manufacturing and the finished product.
  • Implement a Quality metrics to track overall system performance
  • Support new device development including design control 
  • Inspect & test materials, equipment, processes & procedures to ensure quality specifications & safety standards are met.
  • Interface with manufacturing, R&D and product development teams 
  • Share data and learnings that can be used to ensure continuous process and design improvement
  • Coordinate change control & validation projects
  • Foster a quality culture to ensure quality in manufacturing and the finished product.

Knowledge, Skills and Experience Required for the Role:

  • 10 + years’ experience in quality engineering / quality assurance in a microelectronics, photonics or medical device manufacturing
  • 5+ years experience in a leadership role
  • Degree in quality, industrial, or mechanical engineering
  • Working knowledge of ISO 13485:2016, ISO 14971 and MDR
  • Understanding of medical device manufacturing environment*
  • Eligible to work in EU

For a confidential discussion and more information on the role contact Courtney Russell

courtney.russell@collinsmcnicholas.ie

+353 (0) 71 9108062