Senior Regulatory Affairs Manager (UK/Ireland)

Perrigo London, England Posted apr 6, 2026

Full Time
Hybrid
Senior

Job description

As a Senior Regulatory Affairs Manager (UK/Ireland), the work centres on overseeing the company’s regulatory application process to obtain all necessary permits, licenses, certificates, authorizations, etc. It would suit someone who can bring strong professional approach to the role.

Where the work sits

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 particula. 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.

How the role works day to day

Overseeing 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. Provide advisory to company’s management on emerging regulations and developments in industry, particularly in the field of medicinal products and medical devices.

What helps in this setting

Strong professional approach.

Practical details

  • Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supporte.
  • We love our offices and the setting they provide for in-person collaboration and celebration.
  • But we also appreciate the opportunity to work remotely can energise you too, so we promote flexibility with the ability to work two days a week from home in many roles.
  • (The SAVE button will only save your profile information but not submit an application for this open position.) Thank you.

What needs to be in place

  • Ensure company’s regulatory affairs activities are conducted according to relevant regulations,laws, and standards.
  • 8 years Regulatory Affairs, ideally within UK OTC including Post Marketing Licence Maintenance activities, renewals and safety updates.
  • A scientific degree in a pharmaceutical, chemical or biological discipline.
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