Regulatory Affairs Specialist

6 days ago


Beijing, Beijing, China Novo Nordisk Full time

Are you passionate about driving innovation in the pharmaceutical industry? Do you want to make a meaningful impact on the lives of patients? We're seeking a highly motivated and experienced Regulatory Affairs professional to join our team at Novo Nordisk.

The Role

  • Develop and implement regulatory strategies to ensure compliance with global regulations and guidelines.
  • Lead the preparation and submission of regulatory documents, including dossiers and variations.
  • Collaborate with cross-functional teams to ensure regulatory requirements are met throughout the product lifecycle.
  • Provide regulatory expertise and guidance to internal stakeholders.
  • Stay up-to-date with changing regulatory landscapes and ensure our products remain compliant.

Requirements

  • Relevant graduate degree in a field such as pharmacy, pharmacology, or biology.
  • Fluency in English, both written and spoken.
  • Minimum 3 years of experience in the pharmaceutical industry or related field.
  • Proven track record of regulatory compliance and experience with international pharmaceutical companies.
  • Strong analytical and problem-solving skills, with the ability to work independently and as part of a team.

About Novo Nordisk

We're a global healthcare company dedicated to making a difference in the lives of people with chronic diseases. Our mission is to drive innovation and improve the lives of patients through our products and services.

Working at Novo Nordisk

We're committed to creating an inclusive culture that celebrates diversity and promotes equality of opportunity for all our employees. We believe that a diverse and inclusive workplace is essential for driving innovation and delivering exceptional results.



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