Regualtory Affairs Manager - Certifications
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 Antwerpen Belgium.
Our client is an european based, young medical devices company with focus on innovative products.
ROLE DESCRIPTION
In this role you will help our client to obtain certifications for their products (medical devices) and ensure the compliance of submissions with regulatory standards.
RESPONSIBILITIES
- Ensure completeness and compliance of submissions
- Main contact for regulatory authorities
- Develop the process for certifications regarding efficiency
- Closely collaborate with different departments
REQUIREMENTS
- Experience with medical device certifications and regulatory authorities
- Minimum of 3 years relevant experience
- Fluent in English and dutch
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.
