Fresenius Medical Care seeks a Regulatory Affairs & Pharmacovigilance Specialist to lead regulatory activities for the UK across the full product lifecycle. You will ensure compliance, support registrations and post-market surveillance, and provide regulatory guidance to cross-functional teams.
The role is full-time hybrid (40 hours/week) with UK hours; 3–4 years in regulatory affairs/pharmacovigilance, strong GxP knowledge, and collaboration skills are required.
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Regulatory Affairs & Pharmacovigilance Specialist UK — Hybrid employer: Fresenius Medical Care
Fresenius Medical Care is an exceptional employer, offering a flexible working environment that allows you to balance your personal commitments while making a meaningful impact in the lives of patients. With a strong focus on employee development and a commitment to equal opportunities, you will find ample growth opportunities within a supportive team culture that values your contributions. Join us in our mission to provide top-quality dialysis services and enjoy the benefits of working for a market leader in healthcare.
