Hobson Prior are currently looking for a European Regulatory Affairs Manager (Radiopharmaceuticals) to join a fantastic medical devices organisation on a permanent basis located in Surrey. Our client is focused on delivering radiopharmaceuticals.

Please note that to be considered for this role you must have the right to work in this location.

Key Responsibilities:

• For this role, you will handle marketing authorisations and variations of current MA for medicinal products within the EU and UK.
• The ideal candidate will prepare and file regulatory proposals in compliance with regulations.
• Responsible for developing regulatory methods and execution plans.
• Uphold MA and execute RA policies for regulatory compliance.
• Assist with the QPPV by offering information and evaluating documents.
• Execute process changes as needed by PV regulations.
• Prepare and file safety-linked variations.
• Any other assigned duties.

Requirements:

• Educated to a degree level in a life science field.
• Demonstrable experience with pertinent regulatory affairs.
• Able to resolve issues.
• Communication skills both verbally and in writing.
• Expertise on regulatory needs throughout the value chain.
• Know-how of both UK and EU GMP and RA needs.
• Familiarity with conversing with European authorities.

Apply now:

If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.