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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,…
* Follow up on complaints
* Write new SOP’s
* Ensure MDR / IVDR are followed

Requirements:

* Master Degree in Life Science or equivalent by experience, scientific degree not required
* First experience in QA / Quality related role in the pharmaceutical or medical device industry
* Knowledge of MDR and ISO 13485 is a plus
* Fluent level of Dutch, French and English

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.

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About Our Client: We are working on behalf of a renowned organization to find top talent for this exciting role. Partnering with us means gaining access to exclusive opportunities and expert support in advancing your career goals.

We are NonStop, a leading provider of staffing solutions throughout Europe and now also in the US. We're passionate about connecting talent with opportunity and work non-stop to support our clients in hiring the best talent for their teams. Feel free to pop over to our website, NonStop Consulting (https://www.nonstopconsulting.com), for more information, to browse all our roles, or to let us know how we can help you.