Expiry Date: 30-08-2020
Category Regulatory Affairs
Salary: On Application
Job Type: Full Time
Windsor and Maidenhead
We are recruiting for a Global Regulatory Affairs CMC Lead - Biologics for a global Biopharmaceutical company in the UK.
This is a permanent role for an experienced Regulatory CMC professional to become a GRL CMC, Associate Director/Director Grade. With an R&D driven Biopharmaceutical organization based in the M4 Corridor or Berkshire.
This is an exciting role where you will get the opportunity to provide regulatory CMC leadership on cross functional teams, plan and define the regulatory CMC strategy for large molecules in assigned regions.
Who is our client?
Our client is a successful biopharmaceutical company with a strong pipeline of 20 plus molecules and a number of successful drugs on the market. This company has a proven track record of transforming patients’ lives through advanced therapies. This is a global organization and you will work in an international environment where English is the business language.
We ask you to consider the following requirements:
In return you will:
To apply for this role, please press the red “Apply for position” button, or contact Oli Dimitrov on +44 (0)207 801 3388 or Theo Moore on +44 (0)207 801 3384 in full confidence to receive more details on this role or to hear about other available opportunities in Regulatory Affairs.
Note: My client has committed to do digital hiring using Skype (VC), and has a new digital on-boarding and induction training process in place to allow a smooth transition during MERS-COV-2 outbreak. During the next period, new hires will be allowed to work from home full-time, until such a time occurs when normal working returns.
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