| ¸ðÁýºÎ¹® |  | Medical device RA specialist | 
						
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							| ¸ðÁýÀοø |  | 0¸í | 
						
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							| ¾÷¹«³»¿ë |  | 	Prepare submissions for the new product registration 	Initiate, track and facilitate new product registrations and achieve on-time approvals ( from sending POF to approval)
 	Ensure maintenance of registered product license (variation, re-evaluation. GMP renewal)
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							| Áö¿øÀÚ°Ý |  | •	At or above graduation of 4 year university •	Preferred majors in priority: medical science, biology, engineering etc.
 •	Minimum 3 years in regulatory affairs of medical device
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							| ±Ù  ¹« Áö |  | ¼¿ï | 
						
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							| ¿¬......ºÀ |  | Nego. | 
						
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							| ¸ðÁý±â°£ |  | ~15.11.20±îÁö | 
						
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							| ÀüÇü¹æ¹ý |  | 1Â÷ ¼·ùÁ¢¼ö 2Â÷ ¸éÁ¢ÁøÇà | 
						
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							| Á¦Ãâ¼·ù |  | ¿µÇÑ À̷¼¹× ¾÷¹«Á᫐ ÀÚ±â¼Ò°³¼ | 
						
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							| ´ã......´ç |  | °í ÀçÀÍ | 
						
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							| ÀüȹøÈ£ |  | 010-8636-5759 | 
						
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							| ±âŸ»çÇ× |  | •        À̸ÞÀÏ : jiko01@kohuman.com <br /> •        È¨ÆäÀÌÁö : www.kohuman.co.kr<br />
 •        Á¦Ãâ¼·ù : ¿µ¹®À̷¼ ¹× ¾÷¹«Á᫐ ÀÚ±â¼Ò°³¼(À̸ÞÀÏÁ¢¼ö¿ä¸Á)<br />
 •        ÁøÇà°úÁ¤ : 1Â÷ ¼·ùÁ¢¼ö 2Â÷ ¸éÁ¢ÁøÇà<br />
 •        ´ã´çÀÚ: °í.ÈÞ¸Õ ¿£Áö´Ï¾î¸µ °í ÀçÀÍ : 010-8636-5759 <br />
 02)597-1780~1 Fax : 02)597-1782
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							| ȸ»ç¼³¸í |  | ¿Ü±¹°è Á¦¾àȸ»ç | 
						
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