[¿Ü±¹°è Á¦¾à»ç] Sr. RA Specialist
´ã´ç¾÷¹« - - 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
ÀÚ°Ý¿ä°Ç - - 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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- - À̸ÞÀÏ : associate@dreamhr.com******@*******.***
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