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A mid-sized pharmaceutical company is seeking a Regulatory Affairs Manager to oversee post-approval activities across the UK and EU. This role offers the chance to work in a broad regulatory capacity, contributing to a diverse product portfolio while enjoying competitive salary and hybrid work flexibility.
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.