[KOREA] Regulatory Affairs Manager at Santen

Seoul, , South Korea -

Full Time

Start Date

Immediate

Expiry Date

19 Jan, 26

Salary

0.0

Posted On

21 Oct, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Regulatory Affairs, NDA Registration, Korean Legislation, Medicinal Products, Change Control Evaluation, Artwork Development, Regulatory Strategy, Collaboration, Lifecycle Management, Medical Devices, Pharmacy, Science, Documentation Preparation, Timely Response, Variation Management, Approval Process

Industry

Pharmaceutical Manufacturing

Description

Company Description 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. Job Description 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 Bachelor's 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. We aspire to contribute to the realization of “Happiness with Vision” by providing eye health products and services to patients, consumers, and medical professionals around the world. Guided by our CORE PRINCIPLE, “Tenki ni sanyo suru”, Santen is engaged in the global research & development, manufacturing, and sales and marketing of pharmaceutical products in ophthalmology. 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

Responsibilities

The Regulatory Affairs Manager will prepare and submit Korean applications for NDA and variations for Santen Korea, ensuring compliance with Korean HA requirements. The role involves developing regulatory strategies and collaborating with functional teams to enhance business opportunities.