I am currently resourcing for a Manager within Regulatory Affairs. This is a permanent position.
This is working with a Global pharmaceutical company, with Head Quarters in London.
In this interesting and diverse role, you will be responsible for regulatory activities in line with Competent Authority regulations, focusing on development of products for CNS. This may include activities associated with Contract Research Organisation's, as well as ensuring that all documents for regulatory applications are prepared in accordance with company SOPs, GCP and other guidelines.
The Manager will perform many of the functions that a Global Regulatory Representative would perform on one or more projects. This includes participation in international project teams, provision of regulatory advice, registration dossiers and documentation for new products.
This position has become available due to the extensive expansion of my clients R&D business recently. You will be provided opportunities for personal growth, a collaborative and inclusive work environment and exceptional employee benefits. My client rewards high achievement with recognition, opportunities and excellent remuneration.
***Please contact me as soon as possible about this position, the closing date is this week***
This is a fantastic opportunity to join a growing organisation at an exciting time of change and growth and to gain regulatory experience in a truly international environment.
If you are highly motivated, committed and looking for your next career move, call me without delay for a further discussion, I look forward to hearing from you.
Michelle Jackson (Regulatory Affairs Consultant) + 44 1273 727 930 alternately you can email email@example.com
With over 7 years experience in recruitment and outsourcing Michelle specialises in Regulatory Affairs for the pharmaceutical industry. Stelfox - 13 months ago