0¢Ã ä¿ë Æ÷Áö¼Ç : Á¦¾à»ç¾÷ºÎ Sr. RA Specialist
< Primary Job Function >-Registering new products and managing existing products by leveraging a current and changing regulatory environment.-Liaising, responding to, and negotiating with regulatory authorities.-Support business planning activities by providing of smart registration strategy.-Compliant with the current ** procedure.-Leading regulatory compliance management.< Core Job Responsibilities >-Achieve registration approval for planned new products and ensure subsequent maintenance of existing drugs on time.-Provide the best registration strategy and timeline and communicate it with stakeholders.-Secure product license maintenance according to local regulations and global ** compliance standards.-Understand the regulatory environment changes and prepare for the implementation in compliance with the new regulation and ** procedures.-Provide proper and exact Regulatory related information to stakeholders.-Maintain well-managed external communication with related Health Authorities.-Review registration requirements upon request by internal stakeholders.-Leading regulatory compliance management: regular monitoring & implementing actions for RA systems as trainer level. Analyzing regulations and environment, and keeping stakeholders updated.< Position Accountability / Scope>-Product/Business license registration, maintenance, and relevant regulatory activities for Pharmaceutical Products (chemical & biologics).-Communication with the global and local stakeholders regarding the RA topics.-Promotional material review for the assigned products.-Compliance with the **procedures, performing the related activities.< ÀÚ°Ý¿ä°Ç >- ´ëÁ¹ÀÌ»ó (¾àÇÐ ¿ì´ë / °ü·ÃÀü°ø ¼±È£ )- ´Ù±¹Àû±â¾÷ °æ·ÂÀÚ ¼±È£- Á¦¾à»ç¾÷ RA 7³âÀÌ»ó ~- ¿µ¾î »ó±Þ¢Ã ÀüÇü¹æ¹ý : ¼·ùÀüÇü>¸éÁ¢(1Â÷½Ç¹«/2Â÷ÀÓ¿ø)>OFFERÇùÀÇ>ÃÖÁ¾°á°ú¹ßÇ¥¢Ã Á¦Ãâ¼·ù : ¿µ¹®(Çʼö) À̷¼ ¹× °æ·ÂÁ᫐ ÀÚ±â¼Ò°³¼ (MS¿öµå Çü½Ä)¢Ã Á¦Ãâ¹æ¹ý : ymlim@plus-hr.co.kr******@*******.*** ·Î À̸ÞÀÏ Á¢¼ö-. ÃÖÁ¾¿¬ºÀ, Èñ¸Á¿¬ºÀ ÇÊÈ÷ ±âÀç-. ÷ºÎ Ç¥ÁØÀ̷¼¾ç½Ä »ç¿ë ±ÇÀå