I have a role as RA QA Officer Benelux for a dynamic medical device company where you will support the RA/QA Manager in a variety of activities. The company has a big portfolio of medical devices with different levels of risk so you will have a variety of tasks in as well Regulatory as Quality and find a challenge in coordinating and prioritising your activities.
Responsibilities:
* Support and maintain the Quality Management System (QMS) under ISO 13485
* Support the set up of the Belux Quality Management System (QMS)
* Ensure follow up on non-conformance, CAPA’s, x2026;
* Follow up on complaints
* Write new SOP’s
* Ensure MDR / IVDR are followed
* Provide internal trainings
Requirements:
* Master Degree in Life Science or equivalent by experience, scientific degree not required
* First years of experience in Quality Assurance or Regulatory Affairs for the medical device or pharmaceutical industry
* Knowledge of MDR and ISO 13485 is a plus
* Fluent level of Dutch and English, French is a plus
Benefits:
* Market rate basic salary
* Attractive extra benefit package
* Flexibility to work home based some days per week
If this job appeals to you please apply here or on the NonStop Consulting website or send it to me, Annelies De Baere, on my Linkedin. If you are not available but you know someone that would be interested, please forward this to them and help the people in your network.
NonStop is one of the largest and fastest growing specialised life-sciences & Med-tech recruitment companies in Europe. We are proud members of the APSCo life sciences group who ensure we meet the highest quality standards within the recruitment industry. Our offices are located in the UK, Switzerland, Romania, Luxembourg, US and the Czech Republic and we hold labour leasing licences for all EU8 countries. our website for a full list of the niche markets we cover.
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