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Regulatory Affairs Specialist
1 month ago
As a Regulatory Affairs Manager at Novo Nordisk, you will be responsible for ensuring compliance with regulatory requirements for new products, license renewals, variations, and deregistrations. This includes planning and executing regulatory submissions, managing regulatory systems, and collaborating with cross-functional teams to ensure regulatory influence.
QualificationsTo be successful in this role, you will need a relevant graduate-level degree, such as Pharmacy, Pharmacology, or Biology. You must also have fluency in both written and spoken English, as well as a minimum of 4+ years of experience in the RA area in the pharmaceutical industry. Additionally, you should possess team working characteristics, knowledge of Novo Nordisk's mission and vision, and active and creative thinking abilities.
We are committed to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk, we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world, and we know that this is only possible with talented employees with diverse perspectives, backgrounds, and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve, and the communities we operate in.
