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Regulatory Affairs Specialist

1 month ago

Beijing, Beijing, China Novo Nordisk AS 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 A/S.

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 and support to ensure the quality and integrity of our products.
  • Stay up-to-date with changing regulatory requirements and ensure our products meet the highest standards.
  • Contribute to the development of regulatory policies and procedures to ensure compliance and efficiency.

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 the Department

Our Clinical Medical Regulatory and Quality (CMRQ) department is dedicated to bringing our products to the Chinese market with speed and quality. We're a team of experts who are passionate about making a difference in the lives of patients. If you're looking for a challenging and rewarding role that will allow you to grow and develop your skills, we'd love to hear from you.