Regulatory Affairs Specialist

2 weeks ago


Beijing, Beijing, China Novo Nordisk AS Full time
Key Responsibilities

As a Regulatory Affairs Manager at Novo Nordisk A/S, you will be responsible for ensuring compliance with regulatory requirements for new products, license renewals, and variations. This includes planning and executing regulatory submissions, managing regulatory systems, and collaborating with cross-functional teams.

Qualifications

To be successful in this role, you will need a relevant graduate-level degree in a field such as pharmacology or biology. You must also have fluency in written and spoken English, as well as a minimum of 4+ years of experience in the pharmaceutical industry. Additionally, you should possess strong team working skills, knowledge of Novo Nordisk's mission and vision, and the ability to think creatively and strategically.

We are committed to creating an inclusive culture that celebrates diversity and promotes equality of opportunity for all employees, patients, and communities. If you are a talented and motivated individual who is passionate about making a difference in the world, we encourage you to apply for this exciting opportunity.



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