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1. Validation Strategy & Execution
Validation Master Plan(VMP) ¼ö¸³ ¹× Á¤±â ¾÷µ¥ÀÌÆ® Process Validation (Aseptic Process Simulation Æ÷ÇÔ), Cleaning, Computerized System Validation °èȹ ¹× ½ÇÇà Equipment / Facility / Utility Qualification ¼öÇà Validation °ü·Ã SOP ÀÛ¼º ¹× °³Á¤ 2. Project Management
ÇÁ·ÎÁ§Æ® ´ÜÀ§ Validation / Qualification Àü·« ¼ö¸³ ¹× ½ÇÇà Cross-functional Çù¾÷À» ÅëÇÑ ÀÏÁ¤ ¹× ǰÁú °ü¸® 3. Documentation & Compliance
Validation Protocol / Report °ËÅä ¹× ½ÂÀÎ GMP ¹× ±Û·Î¹ú ±ÔÁ¦ ¿ä°Ç ±â¹Ý Validation ÇÁ·Î¼¼½º ¿î¿µ ³»ºÎ/¿ÜºÎ Audit ¹× ±ÔÁ¦±â°ü ´ëÀÀ 4. Operation Excellence
Validation ÇÁ·Î¼¼½º °³¼± ¹× È¿À²È ÃßÁø 5. Team Leadership
ÆÀ Àη ¿î¿µ ¹× ¾÷¹« ¹èºÐ ÆÀ¿ø ±³À° ¹× ¿ª·® °³¹ß ³»ºÎ À¯°üºÎ¼ ¹× ¿ÜºÎ ÆÄÆ®³Ê Çù¾÷ ¸®µù
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Çлç ÀÌ»ó (Á¦¾à, ¹ÙÀÌ¿À µî °ü·Ã Àü°ø) QA Validation °æ·Â 13³â ÀÌ»ó FDA ¹× ±Û·Î¹ú ¼öÁØ Quality System ¿î¿µ/°³¼± °æÇè (5³â ÀÌ»ó) GMP ¹× Validation Àü¹Ý¿¡ ´ëÇÑ ±íÀº ÀÌÇØ ¿µ¾î Ä¿¹Â´ÏÄÉÀÌ¼Ç °¡´É (ºñÁî´Ï½º ÀÌ»ó ¼öÁØ) ±Û·Î¹ú ÇÁ·ÎÁ§Æ® ¶Ç´Â Audit ´ëÀÀ °æÇè ¿µ¾î Ä¿¹Â´ÏÄÉÀÌ¼Ç ¿ª·®
[ ÀüÇü¹æ¹ý ] 1Â÷ ¼·ùÀüÇü 2Â÷ ¸éÁ¢ÀüÇü
[ Á¦Ãâ¼·ù ] ±¹¹®.¿µ¹®À̷¼.°æ·Â±â¼ú¼ Æ÷ÇÔ (°¢Á¾ Áõºù¼·ù´Â ¼·ùÀüÇüÇÕ°ÝÀÚ¿¡ ÇÑÇØ ÃßÈÄÁ¦Ãâ) À̸ÞÀÏ: carly.lee@peoplework.co.kr******@*******.*** ä¿ë´ã´ç : ÀÌ°æ¾Æ Àü¹« ( ***-****-****/ ***-****-****)
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[ÀÚ°Ý¿ä°Ç] °æ·Â: °æ·Â 13³â¡è ÇзÂ: ´ëÁ¹ Á÷¹«±â¼ú: ǰÁú°ü¸®, ǰÁú°ü¸®QA, Á¦¾à, FDA, QA, »ý»ê°ü¸®
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