Expiry Date: 12-12-2020
Category Regulatory Affairs
Job Type: Full Time
Regulatory Affairs Snr Associate for a Global Medical Devices role, Belgium!
Location: Ghent, Belgium
We are looking for a candidate who wants to develop their regulatory affairs expertise in a diverse and dynamic working environment, where you will be challenged to operate in a fast paced and commercially focused environment where you will receive great career development and “hands on” training.
Your main objective will be to work on Global Regulatory Affairs projects, as a Regulatory Affairs Snr Associate supporting business needs in the medical device area including new product developments, roll-outs and maintenance projects, ensuring compliance with EU Medical Device Directive/EU Medical Device Regulation & other related regulatory requirements including relevant ISO standards.
This is a great new position within a strong and dynamic International Regulatory Affairs team and this is a very nice opportunity to join a successful and growing global consumer health care organisation and be part of a diverse and well respected Regulatory Affairs function.
The ideal candidate will ‘Give it a go’ and have a “positive attitude” and be strong when it comes to creative and problem solving thinking whilst being thorough and focused with the necessary attention to detail. You will need the ability to work on several projects in parallel in a flexible manner both autonomously and in a team environment…. with a passion for regulatory affairs.
If you have at least two years hands-on regulatory experience in a consumer product related EU regulatory environment with experience in either OTC, chemicals, biocides and/or cosmetics legislation, and want to grow your experience as well as your career….. then we want to hear from you!
To apply for this role, please press the red “Apply for position” button, or contact me, Theo Moore on +44 (0)207 801 3384 for an initial discussion about the role and other projects.
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