[Innovative Medicine] R&D, Associate Director, RA Policy & Intel Japan, Regulatory Policy Intelligen

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Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.

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POSITION SUMMARY:


* Drive and manages the activities of Regulatory Intelligence as the representative of Japan RA and related Japanese function within R&D, such as proactively driving Industry Association or Health Authority (HA) interactions to successfully develop the Janssen compounds or raise Japanese presence among industry or to HA.


* Lead and administrate the strategical discussion from the perspective of the contribution to both of public health and our business.


* Lead the identification of regulatory and legislative trends and issues that have the potential to impact the development and marketing of pharmaceutical products within Japan and provide high quality strategic input aimed at influencing the future regulation.


* Japan Regulatory Policy Lead to engage in direct regulatory advocacy and influencing activities relating to regulatory healthcare policies partnering with stakeholders including local subject matter experts and AP/GRPI .


* This is accomplished through a variety of activities, including participation in Trade Association initiatives, Health Authority meetings and consultation as well as contribution to commenting on new legislation and guidance.

PRINCIPAL RESPONSIBILITIES:


* Regulatory Policy Japan Expertise
+ Provide leadership for proactive & reactive policy development internally and externally
+ Provide leadership for key Trade Associations and Professional Organizations
+ Provide expert advice on and interpretation of key regulatory policy issues affecting local environment
+ Develop effective approaches to and participate in Trade Association Committees and Initiatives, Professional Organizations activities and Health Authorities meetings and consultations.


* Advice and Cooperative to RCLs activities for policy focused projects (ex, Regenerative medical products etc)
+ Attend and provide feedback to RCLs and R&D members on current regulatory guidelines and procedures as well as emerging regulatory/legislative issues that impact or affect products.
+ Attend and provide feedback to RCLs and R&D members on local regulation of new business area.
+ Collect opinions from R&D activities and liaise with Trade Associations to bring them up to Working Group with HAs


* Cooperative to regulatory policy and intelligence based on Japan regulation to AP/GRPI, R&D and JJ MedTech
+ Collaborate ...