Lead Regulatory Affairs in Japan and grow your career within a dynamic, international team. You will be the driving force behind regulatory submissions in Japan, working closely with Japanese authorities and internal stakeholders. You will play a key role in ensuring compliance and facilitating the successful launch of new products. This role offers the chance to make a significant impact on the company's success in the Japanese market while developing your expertise in regulatory affairs.
業務内容:
Lead the preparation of applications, partial change applications, and Class 1 notifications
Prepare and submit QMS documentation as needed
Support Class IV applications and lead consultations with PMDA
Support regulatory assessment of change controls
Manage and maintain Shonin documents
Interact with Japanese authorities and industry groups
Manage reimbursement processes
Review promotional materials and labeling
応募資格:
Minimum 5 years of RA experience in the medical device industry
Class IV experience preferred
Experience with Japanese regulatory processes (PMDA, MHLW)
Excellent written and verbal communication skills in Japanese and English