Santen

Life Sciences

RASpecialist

$58000–82000k ~AI est. Seoul, Seoul, South Korea FULL TIME
The Brief

“RA Specialist at Santen. Skills: Regulatory affairs, Korean regulations, Pharmaceutical registration. Prepare Korean applications for NDA. Submit application for NDA(s) or variation(s) to Korean”

Industry & Context.

Life Sciences

What They're Looking For.

Must Have

Working experience for RA at pharmaceutical company(s) in Korean for more than 3 years, Fluent in Korean and English (Reading, writing and speaking)

Nice to Have

Bachelor degree in Pharmacy, Knowledge of Korean legislation and regulations for pharmaceuticals, Understanding of the registration procedures in Korea for NDA, variations, K-DMF and other regulatory scopes, RA experience in foreign pharmaceutical company(s), Working experiences to register K-NDA and/or variations, Both experiences for NDA and BLA, Experience leading a regulatory project from the beginning

What You'll Do.

Prepare Korean applications for NDA

Submit application for NDA(s) or variation(s) to Korean

Respond to any request of K-HA

Prepare relevant documents to be submitted to HA

Evaluate change controls

Review change control requirements

Monitor local regulations and/or guidelines

Share regulations with relevant stakeholders

Comply with local regulations

Provide regulatory insights to relevant functional members

Create local artworks written in Korean

Monitor new and/or updated KR regulations

Monitor updated guidelines

Monitor updated direction of Korean HA

How You'll Work.

Team & Collaboration

Relevant stakeholders; Relevant functional members

Communication Scope

Reading; Writing; Speaking

Process & Methodology

Regulatory project

Free ATS check

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