Regulatory Affairs Senior Manager for Immunology products, Based in Brussels

Brussels, Belgium
On Application
10 Oct 2019
09 Nov 2019
TM/10449A R2
Theo Moore
Full Time
Contract Type
Experience Level

Regulatory Affairs Senior Manager for Immunology products, Based in Brussels

Dynamic and exciting Regulatory Affairs Senior manager role, covering Immunology development projects. Based in Brussels, supporting clinical and non-clinical activities for all phases of development.

Location: Central Brussels, Belgium

My client organisation is a rapidly expanding medium sized Bio/Pharmaceutical company with an excellent pipeline with a mixture of both NCE’s and NBE’s in all stages of development.  The regulatory department covers Europe, Middle-East and Africa and you will be based at the EU corporate Headquarters, which is the hub of all strategic decision making.

Despite the current EU economic climate, this client is still a growing company. The organization is always exploring, expanding, and adapting to changes and it recognizes excellent performance with promotions and development opportunities internationally, whenever appropriate.

From the EU HQ you will have a friendly and dynamic working environment in state of the art offices that have a number of staff restaurants, offers flexible working hours, dedicated parking, is in close proximity to the train, bus and metro stations, offers good options to work from home, and provides all employees with a highly rated benefits package including comprehensive medical and healthcare insurance for you and your family, as well as lunch vouchers and travel vouchers. A fully comprehensive re-location package (including accommodation and bonus/allowances) is also available if needed.

As a Regulatory Affairs Senior Manager you will be responsible for providing specific regulatory affairs leadership and support for a new brand / portfolio of 6 Biological indications in Phases 2 and 3 of development operating as the EU Regulatory Liaison in a supportive EU Regulatory Affairs team focused on strategy  development & delivery of successful registrations.

This regulatory department really is a great place to work with good individuals and a great management team that will bring the best out of you.  You will be encouraged to strive for continual improvement and development of your technical and managerial expertise whilst working with high value / potential blockbuster indications.  This role comes with fantastic promotion prospects to either AD level or GRL and a real career development plan.

You will need to have at least 5-10 years Regulatory affairs experience in development or MAA activities for EU or International regions and worked in Phase 1 to Phase 3 clinical studies or have experience in Orphan drug disease supporting a variety of related submissions i.e. Orphan drug designation (US, EU), knowledge of paediatric study requirements in either the EU or US or supported HA/Scientific advice meetings.


To apply, please send a full CV to, or alternatively, contact Theo Moore on +44 (0)20 7801 3384. We are assigned these roles by our client and will provide you with support throughout the hiring process.


About Advanced Search & Our Network

Advanced Search, has a network of affiliated companies including ADV Regulatory, and ADV Talent Partners. Together, we are specialists in Regulatory Affairs and Life Sciences recruitment especially around mAbs and biologicals for roles in R&D and Commercialization and have been established and hiring in this area since 2005.

Our team know our subject matter areas and our mission is to help you grow your career each and every step of the way. We have helped many of today's leading companies develop strong regulatory sciences functions and are known for hiring complimentary teams that work well with each other, at owner-contributor, strategy leading and people management levels.

Contact us today to see how we can help you make that next career move on

+44 (0)20 7801 3380

All applications are kept in confidence and we invite applications from all members of the Academic, Research & Development based bio-/pharmaceutical community.

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