Senior Regulatory Affairs Manager (UK/Ireland)

Senior Regulatory Affairs Manager (UK/Ireland)

Perrigo

London, United Kingdom

Description Overview

As a key member of the Europe North Cluster Regulatory Affairs Team, the Senior Regulatory Affairs Manager will have oversight and accountability for regulatory licencing and post marketing regulatory activities for all products marketed within UK & Ireland.

In this role you will be responsible for ensuring strategies and relationships with local authorities align with the business needs of Perrigo Europe North Cluster with a particular focus on UK & Ireland.

Scope of the Role

• Ensure company’s regulatory affairs activities are conducted according to relevant regulations,laws, and standards;
• Oversee the company’s regulatory application process to obtain all necessary permits, licenses, certificates, authorizations, etc.;
• Establish and maintain good relationship with regulatory authorities, trade associations and internal stakeholders;
• Ensure appropriate basis to marketing strategies are identified and/or implemented; assists in identification of advanced regulatory strategies for all regulatory classifications, with focus on medicinal products and medical devices;
• Provide advisory to company’s management on emerging regulations and developments in industry, particularly in the field of medicinal products and medical devices;
• Manage a team of regulatory affairs professionals.

Experience Required

• A scientific degree in a pharmaceutical, chemical or biological discipline;
• 8 years Regulatory Affairs, ideally within UK OTC including Post Marketing Licence Maintenance activities, renewals and safety updates;
• Must have leadership experience, and strong experience in medicinal products;
• Experience from launching new products and interactions with PAGB and ClearCast.