Regulatory Affairs Manager

vor 2 Wochen


Schweiz Merck Sharp & Dohme (MSD) Vollzeit

Job Summary: We are seeking a highly skilled Regulatory Affairs Manager to join our team at Merck Sharp & Dohme (MSD). As a key member of our regulatory team, you will be responsible for managing registered products and registering new products within the agreed timeline.

Key Responsibilities:

  • Communicate effectively with international RA team contacts to ensure seamless registration processes.
  • Prepare and submit registration dossiers and related questions in a timely manner.
  • Follow up on registration procedures to ensure timely completion.
  • Build and maintain strong relationships with key stakeholders to facilitate registration processes.
  • Organize registration evaluation meetings to ensure effective decision-making.
  • Update registration regulations to ensure compliance with changing regulatory requirements.

Requirements:

  • At least 6 years of experience in Regulatory Affairs in the pharmaceutical industry.
  • Experience in Oncology, CDx, or IVD is highly desirable.
  • Proficiency in both English and Chinese communication.

About Us: Merck Sharp & Dohme (MSD) is a leading global healthcare company dedicated to improving lives through innovative medicines, vaccines, and animal health products. We are committed to advancing healthcare and well-being around the world.



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