[±è°æÈñ] [ÃæºÏ±Ù¹«] ¹ÙÀÌ¿À ÀǾàǰ °ü·Ã, QA Validation °æ·Â3³âÀÌ»óÀÚ(¿µ¾î°

Date 07/19/2017   Hits 839

1. ¼Ò¼Ó ÇìµåÇåÆÃ ȸ»ç¸í: Á¦ÀÌ¿¡ÀÌÄ¡¿¡ÀÌÄ¡¾Ë-JHHR
2. ¼Ò¼Ó ÇìµåÇåÆÃ»ç ȨÆäÀÌÁö: http://www.jhhr.co.kr
3. ¼Ò¼Ó ÇìµåÇåÆÃ»ç ȸ»ç ÀüÈ­¹øÈ£: 82-2-567-7405 (Á÷Åë)
4. ¼Ò¼Ó ÇìµåÇåÆÃ»ç ȸ»ç¿ë, À̸ÞÀÏ : jhhr@jhhr.co.kr
5. Æ÷Áö¼Ç ÁøÇà ÇìµåÇåÅÍ¸í ¹× Á÷±Þ : ±è°æÈñ °úÀå

[ÃæºÏ ±Ù¹«] ¹ÙÀÌ¿À ÀǾàǰ °ü·Ã, QA Validation °æ·Â 3³âÀÌ»óÀÚ(¿µ¾î°¡´ÉÀÚ) ¸ðÁý

1.ÀÇ·Ú»ç: ±¹³» À¯¸í ¹ÙÀÌ¿À ÀǾàǰ °ü·Ã ȸ»ç

2.¸ðÁý ³»¿ë : ¹ÙÀÌ¿À ÀǾàǰ °ü·Ã, QA Validation °æ·Â 3³âÀÌ»óÀÚ(¿µ¾î°¡´ÉÀÚ)

¢Ã Position

-Education : minimum Bachelor in (Bio) Pharmaceutical or related Biological sciences

- Minimum 3 years of practical experience in the related area: Proven experience in a Quality department with validation activities in Pharmaceutical company ( international company experience will be appreciate), EU, US and Korean GMP experience is strongly requested, Good Knowledge on Aseptic product manufacturing and clean area design

¢Ã ä¿ë½Ã ¼öÇà ¾÷¹«

- Reviews all validation and qualification documents in Osong Plant 2

- Reviews documents related validation and qualification as equipment manuals, deviation on equipment, calibration certificate

- Supports the validation and qualification activities


¢Ã ¿¬ºÀ¼öÁØ ¹× º¹¸®ÈÄ»ý: Çö, ¿¬ºÀ ¼öÁØÀÌ»ó ÃßÈÄ °æ·Â¿¡ µû¶ó ÇùÀÇ °¡´É/ 4´ë º¸Çè µî

¢Ã ±Ù¹«Áö : ÃæºÏ

¢Ã Á¦Ãâ¼­·ù: ±¹¹® À̷¼­(»çÁøÇʼö) ¹× »ó¼¼ °æ·Â±â¼ú¼­(Çʼö)

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

¢Ã ´ã´çÀÚ: ±è°æÈñ °úÀå
¿¬¶ôó : 02- 567-7405
À̸ÞÀÏ : jhhr_kh@naver.com