Our client, a leading global healthcare company based in Tokyo, Japan is currently looking for someone to join their team as a permanent Regulatory Affairs Specialist.
Responsibilities:
- Develop strategies for managing submissions of drug applications
- Ensure timely completion of regulatory documents
- Collaborate with cross-functional teams on submission plans
- Provide guidance on labeling requirements
Qualifications:
- Bachelor's or Master's degree preferably related to life sciences (e.g., Pharmacy)
- Experience working directly with Japanese Pharmaceuticals & Medical Devices Agency
- Understanding of regional/global guidelines pertinent to pharma products
- Bilingual
If you are interested, please apply with your CV attached.
