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1. ¾à»ç¹ý, ÀÇ·á±â±â¹ý ¹× ȸ»ç ³»ºÎ ±ÔÁ¤À» ÁؼöÇÑ Ç°Áú°ü¸®½Ã½ºÅÛ(Quality Management System) °ü¸®
2. GMP(Good Manufacturing Practice), GDP(Good Distribution Practice), ISO13485 µî ¿¡ ´ëÇÑ ÀÌÇØ
3. ȸ»çÀÇ ±¹Á¦ Ç°Áú ±âÁØ ¹× °¡À̵å¶óÀÎ ±¹³» Àû¿ë
4. ³»¿ÜºÎ Ç°Áú°¨»ç(Audit) ´ëºñ ¹× ÀÌ¿¡ µû¸¥ ½ÃÁ¤Á¶Ä¡ ½ÇÇà
5. ÀÇ·á±â±â KGMP(Korea Good Manufacturing Practice) ÀûÇÕÀÎÁ¤¼ °ü¸®
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1. ´ëÁ¹(4³âÁ¦)ÀÌ»ó, ¿µ¾î°¡´ÉÀÚ
2. Á¦¾à / ÀÇ·á±â±â ºÐ¾ß Ç°Áú°ü¸® °æ·Â 4³â ÀÌ»ó ¶Ç´Â ÀÚ¿¬°úÇÐ/°øÇÐ/ÀÇÇÐ Àü°øÀÚ
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1. ±Ù¹« ÇüÅ : Á¤±ÔÁ÷
2. ±Þ¿© Á¶°Ç : ±âÁ¸ ¿¬ºÀ´ëºñ ÇùÀÇ (MAX 6000¸¸¿ø)
3. ±Ù¹« Áö¿ª : ¼¿ï ¿ª»ïµ¿ Bracco ¼¿ï ¿ÀÇǽº
4. ¼±È£ Á÷±Þ : °úÀå±Þ (´ë¸®~Â÷Àå)
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2. 1Â÷ Çѱ¹Áö»çÀå, ÀλçºÎ »ó¹«
3. 2, 3Â÷ Global È»ó ÀÎÅͺä
1. At least 4 years QA experience in multinational company in medicinal or medical device;
2. Experience in manufacturing site or commercial affiliate are both ok;
3. Experience in consumer goods, chemicals, cosmetic will not be considered, QC experience will also not be accepted.
4. Good knowledge and experience of GMP or GDP is essential. Experience of both GDP and GMP is highly plus.
5. Experience in batch release, complaint handling, change control, deviation and CAPA are essential.
6. GXP audit, communications with KFDA, registration is plus;
*¼·ùÁ¢¼öE-mail : kschoi@hrkorea.co.kr
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ÀüÈ : 02-3450-1263
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