EMEA Regulatory Affairs Senior Specialist - Hybrid

Kenvue is seeking a Senior Regulatory Affairs Specialist in Reading, UK. In this hybrid role, you will oversee all regulatory activities associated with EMEA medicinal products. You will prepare submissions, monitor reviews, and ensure compliance with quality system requirements.

The ideal candidate will have at least 6 years of regulatory experience, strong communication skills, and a relevant degree. Enjoy a competitive benefits package, including paid company holidays and development opportunities.