PMS - High-tech Medical Devices - QA

€40000 - €55000 per annum
Oct 14, 2016
Nov 13, 2016
Sophie van Goethem
Jobseeker Type
Organization Type
Contract Type
Full Time

We are looking for a QA professional with experience in Post-Market Surveillance or Complaint handling.

Our client is one of the most advanced high-tech medical devices companies in their field and is part of the big Danahar group. Their growth rates are unrivalled and they doubled in size in 2015. Therefore it is the perfect time to join the company and grow together. It will give you the chance to quickly move up on the career ladder.

In this position you will focus on Post Market Surveillance and Complaint Handling. You will process data from different sources and make sure it all comes together to useful input for the different departments. This also means that you will have a lot of interaction with these different departments throughout the various stages of the product life cycle.

We require someone with a good experience in dealing with post-market surveillance, complaint handling in the medical devices industry. Experience with Pharmacovigilance will be considered as well. You will need a strong technical background to understand complex electronic equipment and software.

The company offers an attractive salary, a super talented team to work with and an inspiring environment. Furthermore, the company is located next to the train station and therefore very easy to reach by public transport from both Antwerp and Brussel. As the company is expanding worldwide there will be many career opportunities for you in the future both on national as well as on international level.

Send your CV in word format to Sophie van Goethem at 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.

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