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QA & RA Officer for medical equipment

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SIRE Life Sciences is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldnt stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment, making sure we, or better yet, you find the right career!


Our client is a professional Medical Devices organization, based in Netherlands.

This client is a market leader that offers products and services that are dedicated to improve the health of our society. There specialty lays in the development of medical monitors and therapies. They have an extensive of scale products in their range varying from thermometers to blood pressure monitors.


You will become part of the subsidiary which is responsible for various continents including Europe and the Middle East. This job has a time period of 3 months and can be extended with 2 additional months. Your primary job is to support the Regulatory Affairs and Quality Assurance team. You will have to establish and maintain relationships with the Quality and Regulatory team. You are the person that interacts and combines the vision of both parties when it comes down to processes. You will control and overview documentation and report whenever there are any discrepancies occurring within these documents and legislation.


Overall, your role will be supportive which requires to collaborate closely with your RA/QA team and other departments within the organisation. Additionally, you will have the following responsibilities:

Interaction and communication with both internal and external stakeholders

Creating awareness of importance RA and QA within the corporate organisation by using internal resources

Providing advice and support to management in set up of QA/RA processes

Controlling and assessment of promotion materials with relevant documentation and product specifications


Bachelor of Science

Minimal 3 years of experience within the Medical devices industry

Minimal 2 years of experience within QA and RA role

Excellent knowledge of regulation and legislation of Europe

Basic understanding of the differences in medical device legislation from other continents

Team player

Fluency both in English and Dutch

Eye for detail and open minded

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Juliette van Kraaij.

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