Company: Skills Alliance
Reference: SKILLSALL RA UK/IR
Closing Date: 16 Dec 16
Salary (£): On Application
A growing pharmaceutical company based in Central London is looking to add a Regulatory Affairs Associate to their UK and IR team to support their...
A growing pharmaceutical company based in Central London is looking to add a Regulatory Affairs Associate to their UK and IR team to support their regulatory submissions. This is a great opportunity for a Regulatory professional to move into a role that offers broad responsibilities and the chance to manage the full product life cycle.
You will be responsible for preparing, collating and submitting regulatory documents including CMC variations and renewals as well as new MAA’s to the UK and IR authorities. You will also be accountable for managing the full product life cycle and liaise with the relevant health authorities to ensure any submission queries are answered in a timely manner.
The successful candidate will be a driven professional who will be able to effectively move projects forward. It is not a necessity to have full product life cycle experience but it is important for the successful candidate to be keen on learning and developing their kills in this area. The candidate will preferably have some CMC, publishing and product compliance experience and must have had interaction with the MHRA.
If you think that you are well suited for this role and would like more details please contact Roberto Esposito, Associate Search Consultant, Regulatory Affairs Europe on 0044 207 220 6219 or click APPLY to send a copy of your CV.
Key Words: Regulatory Affairs / Regulatory Affairs Jobs / Regulatory Affairs Senior Associate / Regulatory Affairs Senior Associate Jobs / Commercial Materials / Regulatory UK Affiliate / Regulatory Affairs Roles / Regulatory UK Affiliate Jobs
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