Regulatory Affairs Specialist

SIRE Life Sciences® - More jobs by this advertiser

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 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!

THE COMPANY

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

Medical Devices company based in Gelderland.

ROLE DESCRIPTION

This Medical Devices company is looking for someone who has experience with submissions. The pre market and market area of RA. Experience with CE is mandatory, 510K would be a plus. If you ever have been in contact with notified bodies and competent authorities as well as Ministries of health is a big plus.

The team consists of 6 QA/RA people.

RESPONSIBILITIES

- CE submissions
- Maybe 510K submissions
- Submissions is Asia

REQUIREMENTS

1 - 10 years experience in RA Medical Devices Pre market

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



SIRE Life Sciences®


Amsterdam, (Netherlands)

Phone: +31 (0)20 658 9800
Web: http://sire-search.com

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Company Profile

19 January 2017
Location: Netherlands Gelderland Gelderland
Salary: Competitive Salary
Work type:
Full time
Sector:
Life Sciences
Profession:
Regulatory Affairs

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