Job Title : European Regulatory Affairs Manager
Location : Madrid, Spain - Hybrid
Remuneration : Competitive salary and package
Regulatory Affairs Manager opportunity working for an established pharmaceutical company that specialises in generic, OTC, and prescription medicines. The business is increasingly growing and is looking for a personable and detail-oriented professional to join the small team and lead several Regulatory Affairs activities for an established generics portfolio.
This role will have a main focus on European submissions through MRP, DCP, and National procedures, and also support UK and IRE submissions.
The position will be responsible for managing regulatory submissions, new registrations, and variations applications for a range of different generic products marketed in the UK, IRE, and Europe.
Responsibilities
Requirements
This position allows for the right candidate to work for a leading generics manufacturer and take charge of UK and European submissions. The role will play a pivotal part in the Regulatory Affairs team and ensure compliance. The role includes some excellent benefits, including a generous bonus scheme.
To apply for this role, you must have the full right to work in Europe, as this employer does not provide sponsorship. For more information, please contact lucy.kirkaldy@cpl.com
Regulatory Manager • Madrid, Community of Madrid, Spain