Temporary Regulatory Affairs Specialist

Bedrijfsnaam: -
Plaatsingsdatum: 10/09/2018
Standplaats: -


SIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences market driven on science, we couldn’t 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 organisation, based in Noord-Brabant Netherlands.The CompanyThey are a professional Healthcare and Medical Devices and operates at an international level. They are one of the leaders in technological developments and innovation.

Role DescriptionIn your role as Regulatory Affairs specialist, you will gain the responsibility to collect, maintain and adjust technical files and relevant documentation. You will have a supportive role in creating awareness and exchange of knowledge about international regulations and changes. In addition, you interact with internal and external stakeholders and you will ensure that they are provided with the required information. Next to that, you are involved in the development of strategic plans which are related to the Regulatory Affairs and the implementation. This project is set for a year and can possibly be extended.

ResponsibilitiesOn a daily basis you are responsible for the collection and implementation of regulations in relation to the specification of various products. Furthermore, your tasks include:
• Active role in maintenance and (new) product registration for particular foreign markets
• Supportive role for both internal and external stakeholders about RA related topics
• Development and assessment of the documentation database
• Development and adjustment of strategic plans and assessment of procedures for
verification and validation projects
• Supporting execution of evaluation and risk management procedures
• Application and implementation of international legislation and documentation

Requirements• Bachelor in Life Sciences
• Minimal 4 years of experience in the Medical Devices sector
• Minimal 2 years of experience in a RA role
• Excellent knowledge of the Medical Device Directive, and preferably the MDR
• Excellent writing and verbal skills in English
• Knowledge of the ISO 13485, particularly the 2016 norm
• Strong analytical skills and eye for detail
• Team player, yet individual operator

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.




Plaatsingsdatum :
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9723 HK
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< 1 jaar (starter)
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