NonStop Recruitment
This job has been posted for more than 30 working days and has expired.

Post-Market Surveillance - Opportunity to develop

Our client is one of the fastest growing companies as they doubled in size last year.

With their headquarters in Belgium, you will be conveniently located right next to the train station.

As they are part of one of the biggest international groups, the development opportunities are endless.

If you are seeking to move up on the career ladder, this is your chance.


In this position you will focus on Post Market Surveillance and complaint handling.

You will process all data and interact with the different QA/RA departments.

Your responsibilities include a high level of interaction with your colleagues next to the analysis of incoming data.


You will need a solid understanding of post-market processes and complaint handling in a regulated industry like pharma, food or medical devices (ISO13485, ISO9001).

As you will work with highly innovative software and active devices, an electronical engineer or IT background is strongly recommended.


The company offers a competitive package, state of the art facilities and career acceleration.

Furthermore you will work in an environment of highly talented and motivated colleagues.


Send your CV in word format to Sophie van Goethem at S.Goethem@nonstop-devices.ch and I will be in touch with you directly or for more information give me a call at +32 240 349 80, internal extension 3250.


NonStop is one of the largest and fastest growing specialised life sciences 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 and the Czech Republic and we hold labour leasing licences across Europe.

Please visit our website for a full list of the niche markets we cover.


As a specialized recruiter I can offer you unique market knowledge in the field of Quality Assurance and Regulatory Affairs for the medical devices industry in the Netherlands.

This is not limited to helping you finding the right role, but also giving you personalized advice on salaries, work conditions and developing a career plan for you.


Key Words: Post Market Surveillance, PMS, Complaints, CAPA, Audits, QA, Quality Assurance, QA Engineer, ISO 13485, 93/42/EEC, EN 60601, software design, AIMD, 90/385/EEC, QMS, Quality Management Systems, Kwaliteitssysteem, Risk Management, Medical Technology, Medical Devices, International.