This candidate has over 7 years of experience in the pharmaceutical and medical devices industry and has developed a deep understanding of the product development cycle from concept, through design and development, to market.
They have experience of working for both large multinational companies and small start-ups and they have managed existing Quality Systems and implemented systems from scratch in electronic and paper- based forms.
Able to provide strategic direction leadership and oversight for all regulatory activities.
Strong working knowledge and experience of applicable EU and UK regulations, directives, and guidance across licensed medicines
Exceptional experience in reviewing, authorising, and managing a fast-paced regulatory affairs departments.
