Senior Regulatory Affairs Specialist – EU/MRP Expert Hybrid

Kenvue in Reading, United Kingdom, is seeking a Senior Regulatory Affairs Specialist. This hybrid role focuses on all regulatory activities for EU medicinal products, including submissions (post-approval and new), handling Health Authority inquiries, post-approval commitments and variations/renewals.

Reporting to the Associate Director Regulatory Affairs, you will work from Reading with a cross-functional team to ensure timely approvals and ongoing compliance across the EU regulatory landscape.

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