Job Description

Regulatory Affairs CMC Senior Manager - Brussels

This is a permanent opportunity for a Regulatory Affairs CMC professional to join our client on their exciting journey. 

• Do you already have post-approval experience, some CTA experience authoring and delivering Regulatory CMC submission documents and now want to do more work in development authoring IMPDs and initial MAA submissions for novel small molecule products?

This Regulatory Affairs CMC role is with an international pharmaceutical company with several blockbusters as well as a strong pipeline of biological and small molecule products coming up in development. This organisation excels as a company because it invests and develops its people. It has been able to foster a culture of innovation, collaboration, creativity and maintain continual high standards. 

This company offers a competitive salary package and the flexibility to work from home 2 days per week in general. However, due to the current circumstances, they are now willing to take on new staff working directly from home, run interviews entirely online and onboard as well as induct people from a distance.  

• Do you want to work in an international environment, leading projects, supporting a new MAA and subsequently moving on to being responsible for the preparation and authoring of Regulatory CMC documents for molecules in development?
• Do you want to have a strong input in the development and implementation of the Global Regulatory CMC strategy?
• Do you want to have the chance to lead the CMC aspects of regional Health Authority interactions?
• Do you want to work in the Global HQ of a successful organisation and be supported by an experienced GRL moving forward in your career? 

If the answer to these questions is Yes, then get in touch.  I am happy to hear from you in confidence and give you more information for your consideration. 

To Apply!

To apply for this role, please press the red “Apply for position” button, or contact Oli or Theo on +44 (0)207 801 3388 or +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.

We provide a high level of service because we believe this matters. Our people place individuals at the Specialist, Expert, Regional and Global Head levels, so if you want some advice on when or how to make your next step, or to understand what that next step might look like, let’s collaborate and explore these ideas with each other. ADV Talent Partners only advertise around 30% of our active roles, so for us to really help you, please Register or call us. We provide permanent and contract roles in the following areas, across the USA, Europe and Asia Pacific. General switchboard number +44 (0)207 801 3380.

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