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È˸£Ò½Ò©¼¯ÍÅ---È˸£ÆÕ¿ËÒ©Òµ£¨Î人£©ÓÐÏÞ¹«Ë¾³ÏƸQA Specialist
       È˸£ÆÕ¿ËÒ©Òµ£¨Î人£©ÓÐÏÞ¹«Ë¾ÊÇÈ˸£Ò½Ò©¼¯ÍÅÔÚÎ人ÉúÎïÒ½Ò©²úҵ԰Ͷ×ʽ¨Á¢µÄ¸ßÖÊÁ¿µÄ¹ú¼ÊÖÆÒ©ÆóÒµ£¬²úÆ·º­¸Ç¶àÖÖ¼ÁÐ͵ÄÃÀ¹ú´¦·½Ò©/·Ç´¦·½Ò©£¬ÃæÏòÅ·ÃÀÖ÷Á÷Êг¡¡£ ±¾¹«Ë¾¾ßÓÐÊÀ½ç¼¶µÄ¹ÜÀíÍŶӺͼ¼ÊõÁ¦Á¿£¬ÓÐÁ¼ºÃµÄÆóÒµÎÄ»¯ºÍ·¢Õ¹Ç°¾°£¬ÌṩרҵÅàѵºÍÓоºÕùÁ¦µÄ´ýÓö£¬³ÏÑû¾«Ó¢¼ÓÃË£¬¹²Í¬´òÔìÊÀ½ç¼¶ÖÆÒ©ÆóÒµ¡£
Located in Wuhan Bio-Pharmaceutical Industrial Park,  PuraCap Pharmaceutical Corporation is a brand new state-of-the-art manufacturing plant invested by U.S. Puracap Pharmaceutical LLC, which is head-countered in New Jersey, USA. We are excellent in the U.S. FDA CGMP manufacturing standards. With world-class management team and technical strength, PuraCap Pharmaceutical has an excellent corporate culture and development prospects.  We invite you to join us and work together to build a world-class pharmaceutical company.
Essential Responsibilities£º
1¡¢To be responsible for batch disposition and has the authority to determine whether finished products are released for marketing or not.
2¡¢To be oversight for monitoring process during all the manufacturing and packaging process, assurance all process and operations in compliance with cGMP regulations and site quality requirements.
3¡¢To review or approve the validation report and quality monitoring during validation process.
4¡¢To be responsible for the annual product review
5¡¢To deal with deviations, changes, complaints related to responsible products
6¡¢Other QA jobs including procedure review  assigned by supervisor
QualificationsÈÎÖ°ÒªÇó£º
1¡¢Bachelor degree or above, majored in pharmaceuticals,chemistry or related sciences. »¯Ñ§ÖÆÒ©Ïà¹Ø×¨Òµ×¨¿ÆÒÔÉÏѧÀú
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3¡¢Excellent English in reading and writing;Á¼ºÃµÄÓ¢Óï¶ÁдÄÜÁ¦
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