Regulatory Affairs CMC Manager or Snr Manager for Biotechnology projects, Brussels

Reference: Oli10480

Expiry Date: 30-10-2019

Category Regulatory Affairs

Salary: On Application

Job Type: Full Time

Location:
Belgium

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Job Description

Regulatory Affairs CMC Manager or Snr Manager for Biotechnology projects, Brussels

We have an opportunity for Regulatory CMC professional to work on biological products for an established Biopharmaceutical company based in Brussels.

We have an opportunity for a Regulatory Affairs CMC professional to work on biological products (mAbs) for an established Biopharmaceutical company based in Brussels, Belgium.

Our client is a leading, science-based Biopharmaceutical company that is expanding its R&D pipeline and has already grown to become a major research driven organization. Over the years our client has brought some state-of-the-art medicines from the laboratory to the patient.

The location in Brussels is easily commutable both by public transport and by car. Our client have some exciting new products coming in Phase II, Phase III (mAbs) and a number of products in early development and are committed to increasing access to high-quality healthcare products where there is an unmet need, around the world. My client currently has 3 roles open to Regulatory Affairs CMC professionals at Manager or Senior Manager Grade. This is a permanent opportunity and the salary is very competitive and includes a good bonus, car allowance and an extensive company benefits package and there is also good flexibility to work 1-2 days a week from home.

Role 1: Working on a global blockbuster - this product has been registered 5 times in the EU and US and is my client’s biggest product. They are looking for someone to join the team and help with market expansion projects for the EU and ROW markets (including China, Japan, Asia-Pac & Lat Am).

Role 2: Working on an Immunology NBE (mAb) which currently has 4 indications going through development, with the 1st MAA planned for 2020, so you will be supporting the MAA/BLA.

Role 3: There are a good number of strong NBE’s in early development, so this will be working on indications in Phases 1 and 2 as the EU Liaison with the chance to stay with your projects until MAA.

If you are looking for your next career step in Regulatory Affairs CMC within Biotechnology, in a broad based and varied role, then this might be the right opportunity for you …!

Looking forward to hearing from you.

 

To Apply!

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.

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