1 อัตรา
3 มีนาคม 2558


Performing audits and product tests in the related areas,
• Medical devices auditing and testing e.g. ISO 13485 / MDD, JGMP, Canadian Medical Device Regulation (CMDR)
• Performing audits ISO 13485 / MDD / specific medical device standards / CMDR.
• Performing ISO 13485 / MDD / specific medical device standards / and GMP inspections.
• Performing in-house and public training for clients (e.g. ISO 13485 / MDD / specific medical device standards / QSR).

คุณสมบัติผู้สมัคร :

Thai citizen or permanent residence (to modify to suit local condition) 28-35 years old.
University degree in science or equivalent in the relevant product or medical area or equivalently in electrical or mechanical or medical engineering, medicine, chemistry, physics, microbiology, pha
A minimum of four years work experience in the relevant production technology. At least two out of four years professional experience including Quality Assurance related activities.
Experience in middle management, design, manufacturing or testing of certain devices / products would be beneficial.
Good command of written and spoken English, confident in common computer applications, negotiation and communication skills with a service mind and team-orientation.
Frequent travel is required.
IRCA registered Auditor / Lead Auditor for QMS would be beneficial.

สวัสดิการ :

- ประกันสังคม
- ประกันสุขภาพ
- กองทุนสำรองเลี้ยง
- โบนัส
- ท่องเที่ยวและสัมมนาประจำปี

111 หมู่ที่ 9 ถ.พหลโยธิน ต.คลองหนึ่ง อ.คลองหลวง ปทุมธานี 12120 025648041 Ext.119 025648042