(Senior) Regulatory Consultants (EU, Reg Ops, CMC)

Be a part of a Queen’s Award winning company

EUDRAC is an expanding regulatory affairs and pharmacovigilance consultancy with offices in the UK, Germany and France.If you are looking for a new challenge and want to work in a varied role, we are looking to recruit a number of Regulatory Affairs Consultants at a junior and senior level due to a number of exciting new projects.

About You

If you have experience in EU Regulatory (either pre- or post MAA), Regulatory Operations or CMC we have a role for you if you are the right fit for our team. Key criteria are an enthusiasm for regulatory affairs, the ability to demonstrate attention to detail, a willingness to learn, proven IT skills and a ‘can do’ attitude.

Why EUDRAC?

* An opportunity to make a difference for patients – work focusses on novel products including ATMPs, often treating orphan diseases.

* Work in a company environment fostering a team spirit and an opportunity for you to make an impact.

* Diversified role and exposure to a variety of projects across a wide area of subjects - scientific advice, PIPs, orphan drug designations and centralised/UK registration procedures (pre- and post-authorisation).