[KOREA] Regulatory Affairs Manager
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Job Location:
Seoul - South Korea
Monthly Salary:
Not Disclosed
Posted on:
30+ days ago
Vacancies:
1 Vacancy
Job Summary
- 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
- Discuss with RA head to develop regulatory strategy for each task and execute it to provide better business opportunities for SKR.
- Collaborate with other relevant functional members for ongoing or planned tasks
- Any others instructed by RA head in SKR
Qualifications :
- Bachelors degree in Pharmacy Science or related field
- 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
- 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
Additional Information :
Please submit the resume in Resume Format template.
Submit in 2 languages please. (Korean & English)
Grow your career at Santen
A career at Santen is an opportunity to make a difference. Through our long-term vision outlined in Santen 2030 we are committed to be a Social Innovator - addressing the social and economic needs of people with visual impairments. We have team members around the world using their diverse talents to unlock new modalities and drive innovations for patient outcomes education and treatment. At Santen we believe in empowering all our team members with flexible ways of working and a highly inclusive work environment.
The Santen Group is an Equal Opportunity Employer. We are committed to building diverse teams and ensuring a safe and inclusive physical and virtual workplace for every one of our team members. All employment decisions are based on business needs role requirements and individual qualifications regardless of race color ethnicity national origin/ancestry religion sexual orientation gender gender identity/ expression age disability medical condition marital status veteran status or any other characteristic protected by law.
If you require any kind of accommodation during our recruitment process please let the recruiter from our team know.
*Please note that team assignments may be subject to future changes
Remote Work :
No
Employment Type :
Full-time
Key Skills
- Proofreading
- Adobe Acrobat
- FDA Regulations
- Manufacturing & Controls
- Biotechnology
- Clinical Trials
- Research & Development
- GLP
- cGMP
- Product Development
- Chemistry
- Writing Skills
About Company
As a specialized company dedicated to ophthalmology, Santen carries out research, development, marketing, and sales of pharmaceuticals, over-the-counter products, and medical devices. Santen is the market leader for prescription ophthalmic pharmaceuticals in Japan and its products now ... View more
