Perrigo is looking for an Associate Professional, Regulatory Affairs within our Medical Device Lifecycle Management team in London. The role supports regulatory activities across the product lifecycle to ensure conformity, documentation compliance, product availability and market access.
You will help with lifecycle management tasks including documentation updates, change assessments, regulatory notifications, registrations/listings and maintaining regulatory records, working with
#J-18808-LjbffrMedical Device Regulatory Affairs: Lifecycle Specialist employer: Perrigouk
Perrigouk is an exceptional employer that values innovation and collaboration, providing a dynamic work environment in the heart of London. Employees benefit from competitive compensation packages, including bonuses and a company car, alongside opportunities for professional growth through training and development initiatives. With a strong focus on fostering client relationships and enhancing product knowledge, Perrigouk empowers its team to make a meaningful impact in the healthcare sector.
