QA - Active Devices - Software

€50000 - €70000 per annum
Oct 17, 2016
Nov 16, 2016
Sophie van Goethem
Jobseeker Type
Organization Type
Contract Type
Full Time

We are looking for QA professionals with a strong technical background in active devices, electronics and software.

Our client is one of the notified bodies in Europe with a strong international network. With the upcoming new Medical Device Directive and changes in the ISO13485 they have a busy future and are looking to expand their team with professionals that have a lifelong experience in active medical devices.

In this position you will receive an initial 6-12 months training where you will learn all the ins and outs of being an auditor. In the next stage you will start working alongside a seasoned auditor to show you the tricks of the trade. On your own pace you will start working independently and developing your own client base.

We are looking for people that have a minimum of 5 years experience with QA and/or Regulatory Affairs within the medical devices industry. Furthermore it is essential that you have a solid technical knowledge of electronics and software. Experience with IVD is a bonus.

The company offers free training, workshops, attendance to conference, international business development and the chance to create your own brand and name in the industry.

This is your chance to conquer the industry! 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 +31 207 0910 70, 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: Quality Assurance, QA, Kwaliteit, ISO 14971, ISO 13485, QMS, Quality Management Systems, Kwaliteitssysteem, Risk Management, R&D, Research and Development, Medical Devices, Netherlands, Nederland, International, Auditing, Medical Device Regulation, MDR, 90/385/EEC, 93/42/EEC, 98/79/EC, MDD, AIMD.

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