Overview:
Our client, a mid-sized pharmaceutical company with a growing generics and specialty portfolio is looking for a Regulatory Affairs Manager to lead post-approval activities across the UK and EU.
Key Responsibilities:
Manage post-marketing submissions including variations and renewals
Maintain regulatory dossiers and ensure compliance across markets
Liaise with supply chain and manufacturing for labelling compliance
Support IDMP and eCTD implementation
Requirements:
5+ years in EU regulatory affairs
Experience in post-approval lifecycle management
Knowledge of MHRA processes and EU requirements
Why Join?
Work in a broad regulatory role spanning multiple therapeutic areas
Contribute to the ongoing success of a well-established product portfolio
Competitive base salary with hybrid flexibility and development support
Collaborative team environment with strong cross-functional exposure
Equal Opportunities Employer
Axion is an equal opportunities employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
We specialise in recruitment across multiple sectors – let’s talk.
