[Job Description]
− New drug registration
− Product license amendment
− Flu bulk business support Packaging material preparation
− Support batch selection by reviewing the summary protocol
[Qualifications]
− ¾àÇÐ, »ý¸í°øÇÐ Àü°ø ¼±È£
− Good understanding on MFDS regulation and international guidance
− Minimum 3 years experience in regulatory affairs in pharmaceutical companies.(Biological companies is preferred)
[guideline for application]
1. ÀüÇü¹æ¹ý- 1Â÷ ¼·ùÀüÇü(Á¢¼ö ¼øÀ¸·Î °ËÅ俹Á¤)- 2Â÷ ¸éÁ¢ÀüÇü2. Á¦Ãâ¼·ù- ±¹¹®/¿µ¹® À̷¼ (°æ·ÂÁß½É)- °¢Á¾ Áõºù¼·ù´Â ÃÖÁ¾ÇÕ°ÝÀÚ¿¡ ÇÑÇØ ÃßÈÄÁ¦Ãâ3. Á¢¼ö¹æ¹ý- À̸ÞÀÏ : jennifer@careercare.co.kr
[contact information]
ä¿ë´ã´ç : Ȳ¹®ÁÖ ÀÌ»ç
- Tel : 02-2286-3981, 010-6396-0497- e.mail ÁÖ¼Ò : jennifer@careercare.co.kr
Á÷¾÷Á¤º¸Á¦°ø»ç¾÷½Å°í¹øÈ£ J150002023003