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Corporis Medical is hiring a Trainee Quality Assurance

Are you looking to join a dynamic young medical device company, specialized in developing medical devices for minimal invasive surgery? Do you have what it takes to take full responsibility and ownership to develop a product from concept to market launch? Then this might be just the opportunity you are looking for:

About us

Corporis Medical is an ISO 13485 certified young MedTech company with a focus to improve patients’ lives by minimizing post-operative complications with smarter surgical tools. As such, our focus lies in the improvement of surgery outcomes by developing innovative medical solutions. These solutions will not only improve the safety and efficacy of surgeries but will also ease surgical procedures for surgeons and as a result, save thousands of lives and drastically reduce surgery accompanied healthcare costs.

Key responsibilities include:

  • Maintain HVC Quality Management System according to ISO 13485

  • Assure compliance with all applicable regulations and procedures

  • Support new product design / development and testing with design control, risk assessments and review and by providing QA technical expertise.

  • Review and approve documentation for design history files, technical files and other regulatory submissions

  • Conduct internal audits and external supplier audits and batch records.

  • Maintain and track Corrective and Preventive Actions

  • Provide direct and regular communication to senior management on progress, opportunities & issues



  • BSc or MSc in Biomedical sciences - engineering/Medicine/ Engineering or a relevant field

  • Preferably 1-3 years of experience in the field of medical devices Industry and/or Lifesciences

  • Good understanding of QA and QM systems

  • Understanding of Product development and process development in medical devices

  • proven project management skills

  • Previous experience in (bio)medical domain

  • Understanding of and experience with regulatory approval of medical devices (EU/USA)


If you are interested, please send your application to



Maastricht, the Netherlands

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