Regulatory Affairs Specialist

4 weeks 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 skilled Regulatory Affairs professional to join our team at Novo Nordisk.

About the Role

  • Develop and implement regulatory strategies to ensure compliance with global regulations and guidelines.
  • Collaborate with cross-functional teams to ensure timely and successful product submissions and approvals.
  • Provide regulatory expertise to support business growth and expansion in the Chinese market.
  • Stay up-to-date with the latest regulatory developments and trends in the industry.

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 success in regulatory affairs, with experience in 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 with a commitment to creating innovative solutions for patients. Our CMRQ department is dedicated to bringing our products to the Chinese market with speed and quality, and we're looking for talented professionals to join our team.

What We Offer

We offer a dynamic and inclusive work environment, with opportunities for professional growth and development. We're committed to diversity and inclusion, and we welcome applications from candidates with diverse backgrounds and perspectives.



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