Regulatory Affairs Manager
vor 2 Wochen
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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