Global Submission Officer
Location: BelgiumSIRE 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 West-Vlaanderen Belgium.
The company is a young and innovative producer of medical devices for the healthcare industry.
ROLE DESCRIPTION
In this role you will work in the regulatory affairs team and take part in registration processes for medical devices in Europe, the US and Asia.
RESPONSIBILITIES
- Support the Regulatory Affairs department in submission in Europe, Asia and the US
- Follow up the whole registration process and keep contact with mayor stakeholder (regulatory institutions)
- Post market surveillance
- Advise departments on regulatory aspects
REQUIREMENTS
- B.Sc or higher
- Experience in regulatory aspects of medical devices in an international setting
- Experience with submissions
- English and dutch (fluent)
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Robin Krems.
