Advise medtech companies on regulatory pathways and market entry strategies
Roles/Responsibilities
- Provide guidance on Japan's regulatory requirements for medtech product development
- Conduct feasibility studies for introducing new medical technologies
- Collaborate with R&D teams to align product design with market needs
- Develop go-to-market strategies tailored to Japan's healthcare landscape
- Ensure client projects are delivered on time and meet quality expectations
Required skills
- 5+ years in medical technology consulting or product management
- Familiarity with Japan's medtech regulatory framework
- Strong project management and analytical skills
Preferred skills
- Experience with product lifecycle management in medtech
- Proficiency in data analysis and visualization tools
- Understanding of international healthcare markets
About our client
Life Sciences Big Data Company