LD6592
England UK Generics Regulatory Affairs Consultancy GMP London
Mainland Europe UK UK
Negotiable
5 - 6 Years
Permanent Full-time
See Description
01 278 4703
Linda.Dunne@thornshaw.com
Excellent opportunity to join an Irish owned expanding regulatory consultancy company!
On behalf of our client we are searching for an experienced regulatory affairs professional to fill this challenging role based in central London. The Regulatory Affairs Manager will work within a multidisciplinary team environment to provide regulatory expertise and leadership to other team members. The individual will be responsible for managing and coordinating activities necessary to ensure client company compliance with the requirements of EU competent authorities. On behalf of client companies, the individual will also be responsible for obtaining regulatory approvals for designated marketing authorization applications, product maintenance applications and clinical trial submissions.
Job Requirements:
Bachelor’s degree in pharmacy, a life science or a biomedical discipline.
Over 7+ years experience of the pharmaceutical industry, with 5+ years regulatory affairs experience in a CRO, biotech or pharmaceutical company including demonstrated expertise in EU MAA and CT submissions.
If you are interested in knowing more about this role please email you CV to ldunne@thornshaw.com or call Linda on +353 1 2784671.
Complete confidentiality is guaranteed and your CV will not be submitted to any client without your prior approval.
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Key words: Regulatory Affairs, UK, England, London, Consultancy, Generics, GMP