[¿Ü±¹°è Á¦¾à»ç] Sr. RA Specialist



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  • - Achieve registration approval for planned new products and ensure subsequent maintenance of existing drug on time.
  • - Responsible for the preparation and submission of product registration and get approval from the local health authorities
  • - Maintain Product license aligned with the current in-house specification and MFDS requirements
  • - Monitor and assess the regulatory changes and emerging issues to evaluate the impact in business
  • - Correspondence with Global RA Affiliates

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  • - Bachelor's Degree above (Major: Pharmacy preferred, or other related majors)
  • - 6 ~10 years of relevant experience
  • - 6+ years of experience in RA of the pharmaceutical industry
  • - Experience in multinational pharmaceutical companies preferred
  • - Proficient English
  • - Strong knowledge in of regulatory affairs


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