1) Manage local batch release procedure and external laboratory for OTC/quasi-drug 2) Review and monitor the related regulation for compliance to domestic regulations 3) Quality control & Hygiene management of KGSP for Janssen OTC products 4) Quality compliance management of Distribution Center 5) Self-inspection management and report to Yongin-city Health center 6) Management of AAP on KFDA audit and J&J audit in Korea regarding imported products and DC related 7) Management of QRA with Janssen/external lab/3PL(Yongma) 8) Support consumer complaint management with related team and affiliates 9) NPD support on QA related in OTC/Quasi-drug 10) Manage the deviation and related CAPA regarding imported product as well as KGSP related 11) Support GMP site inspection abroad for registration of J&J products