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Medical device RA specialist |
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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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• 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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Nego. |
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~15.11.20±îÁö |
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010-8636-5759 |
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• À̸ÞÀÏ : jiko01@kohuman.com <br />
• ȨÆäÀÌÁö : 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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