[°ûÁöÇý] ¿ÜÀÚÁ¦¾à»ç, RA(Regulatory Affairs) °æ·Â 3³âÀÌ»óÀÚ ¸ðÁý

Date 10/26/2011   Hits 1030

1. ÀÇ·Ú»ç: ¿ÜÀÚ Á¦¾à»ç

2. ¸ðÁý ³»¿ë : ¿ÜÀÚÁ¦¾à»ç, RA(Regulatory Affairs) °æ·Â 3³âÀÌ»óÀÚ ¸ðÁý

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- 4³â´ëÁ¹ÀÌ»ó
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- ½Ä¾àû Çã°¡, µî·Ï, ´ë°ü¾÷¹« ¼öÇà
- °ü·Ã ºÐ¾ß °æ·Â 3³â ÀÌ»óÀÚ
- Regulatory Input is required at all levels of the pharmaceutical industry.
- The main responsibility of the Regulatory Affairs Team is to plan and execute all activities necessary for the registration of new products and line extension indications.

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¢Ã ±Ù¹«Áö : ¼­¿ï

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¢Ã ÁøÇàÀýÂ÷ : 1Â÷ ¼­·ù ÀüÇü- 2Â÷ ¸éÁ¢ÀüÇü

¢Ã ´ã´çÀÚ: °ûÁöÇý
¿¬¶ôó : 02-567-7407,7408
À̸ÞÀÏ : yskim@jhhr.co.kr