Vice President for Regulatory Affairs Device

Category: Reg Affairs & Safety Pharmacovigilance

Location:Søborg, Capital Region of Denmark, DK

• Spearhead the strategy for RA Device globally in Novo Nordisk.
• Be accountable for the development and execution of regulatory strategies for medical devices and device constituents of the Novo Nordisk combination products in the development pipeline as well as the life cycle management of already approved drugs.
• Inspire, empower, and develop employees with a focus on optimising the way we work, setting ambitious goals and going above and beyond to the benefit of the business and the patients.
• Build and maintain strong relationships with key stakeholders and influence across levels, valuing diverse perspectives.
• Connect with peers in the industry and ensure engagement with relevant industry/pharma associations while keeping up with changing regulatory requirements.

• A Master of Science degree in natural sciences such as engineering, pharmacy, chemistry or similar.
• 15+ years of experience from the pharmaceutical industry, working in a global regulatory function, manufacturing or a function collaborating closely with regulatory affairs.
• 10+ years of robust leadership cultivated within a diverse, international setting and a seasoned leader of leaders with ability to lead and create followership both directly and in a matrix organization.
• Experience interacting with key stakeholders at senior leadership level in production, production development, R&D, commercial and affiliates globally.