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Contract Regulatory affairs Consultant – 6 months contract – Belgium

at Nikolay Dimitrov in Belgium

My client, a Global biopharmaceutical company is currently expanding its Regulatory Affairs – CMC unit. Therefore they are looking for top industry professionals to join their team. On this occasion there is an opportunity for an experienced Regulatory Affairs consultant to join their team of experts in their headquarters in Belgium on a 6 months contract basis with possibility for extension.

This Regulatory Affair Consultant role lies within the CMC regulatory team and you will be involved in preparation, review and submission of CMC variations in EU and US. You will have extensive CMC experience and background in the biopharmaceutical industry and specifically in biologics.

Requirements:
• Strong interpersonal and communication skills
• Relevant regulatory affairs experience - 6+ YEARS in Regulatory Affairs
• Experience in CMC, preferably for biological/biotechnological molecules
• An extensive regulatory background gained in a Biopharmaceutical company
• A good understanding of European and International regulations, procedures and guidelines.
• A degree in chemistry, pharmacy or life sciences

If you are interested in this role or any other regulatory affairs positions, please call Nikolay Dimitrov on 0207 255 6600, or send your CV to Nikolay.dimitrov@secpharma.com


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Published at 16-06-2011
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