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1. Responsible for ensuring that the Quality system is understood and implemented, by monitoring the effectiveness of the quality system and reporting to Korea Branch Management and HQ Group QA/RA
2. Create and implement Korean RA and QA policy in-line with company strategy and local legal requirements
3. Create internal guidelines in order to insure adherence to Korean Pharmaceutical Affairs Law and Korean Medical Devices Law.
4. Monitor changes and reforms within Pharmaceutical Affairs Law (PAL) / Medical Devices Law(MDL) and the Ministry of Health and Welfare (MOHW)
5. Provide product registration support in order to launch products within internal timelines
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5. English proficiency
6. MS office / Hangul word processor
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