Description
We have a senior opportunity for a regulatory affairs professional with more than 8 years of regulatory experience to manage, lead and strategise the regulatory submissions for a late stage biotech product into global markets for a top 20 pharmaceutical company in the Brussels region of Belgium. The role is on a 6 month contract basis (is very likely to extend) and offers a competitive hourly rate. English is the only language requirement.
The product is a biopharmaceutical product however prior biotech experience is not essential for the role, much more important is prior experience with regulatory submissions for Global markets (ie Rest of World/non-European/Emerging Markets) and there is a preference for the APAC region and Japan.
The position will be working closely with global Health Authorities (HA) and affiliates in order to ensure successful and timely submissions of regulatory dossiers. There is a long term strategic element to the role as you will be implementing regulatory strategy submission processes for various global markets.
For this unique opportunity please feel free to apply via this website (with CV or with any questions you may have, a job description is available on request) or call Michael Kellitt on the number provided below. I look forward to hearing from you.
Kind regards,
Michael
Job Code: 99665
Michael Bailey Associates GmbH are acting as a recruiting partner for a global pharmaceutical company in Belgium, please feel free to visit our website for further information on the end client or the role please contact me directly or via application on this website.
Michael Bailey International is acting as an Employment Business in relation to this vacancy.