
KOREA] Regulatory Affairs Manager
- 서울시
- 정규직
- 풀타임
- Santen is a specialized life sciences company with a proud 130-year heritage focused exclusively on ophthalmology. As a Japan-originated, global company with our footprint in over 60 countries, we are dedicated to delivering innovative treatments and digital solutions for eye health and addressing vision-related social issues for people around the world.
- Prepare Korean applications for NDA for new products and variations for approved products of Santen Korea (SKR) allocated by RA head of SKR, and then submit the application for NDA or variation to get the approval from Korean HA by handling supplementary requests of HA accordingly under the supervision of RA head of SKR.
- Respond to any request of K-HA in a timely manner by preparing relevant documents to be submitted to HA on time under the supervision of RA head of SKR.
- Evaluate change controls and review its requirements along with the expected schedule for it under the supervision of RA head of SKR.
- Develop artworks and proceed update of artworks along with relevant variation etc. under the supervision of RA head of SKR.
- Report to RA head for all RA tasks in SKR (Santen Korea) in a timely manner
- Follow up the instruction of RA head in SKR in a timely manner
- Comply with local regulations, guidelines etc. and provide regulatory insights to relevant functional members.
- Prepare applications and/or documents written in Korean under the supervision of RA head in SKR.
- Discuss with RA head to develop regulatory strategy for each task and execute it to provide better business opportunities for SKR.
- Conduct close communication with reviewers in HA for the submitted application
- Ensure timely registration of new products and/or submitted variations
- Create and manage local artworks written in Korean to be complied with local regulation, internal standards etc.
- Review artworks & promotional material
- Monitor local new and/or updated regulations, guidelines, direction of Korean HA etc., and share it with relevant members
- Collaborate with other relevant functional members for ongoing or planned tasks
- Any others instructed by RA head in SKR
- Essential experiences
- Working experiences in Korean regulatory fields more than 7 years
- Working experiences to register Korean NDA for NCE drugs or BLA
- Preferable to have experiences on medical devices
- Essential qualification
- A pharmacist in Korea
- Depth knowledge of Korean legislation and regulations relating to medicinal products
- Depth understanding of the registration procedures and challenges in Korea for NDA and all activities for lifecycle managements
- Skills
- Fluent in Korean and English
- Sufficient knowledge on Korean regulations and pharmacy