QA Manager (for Pharmaceutical Manufacturing Company)

• Generally manage the QA department (with 5 staff) of an EPE pharmaceutical factory (our company exports all products to Japan).
• Take responsibility for working with DAV (Drug Administration of Vietnam) ; or Japanese PMDA (Pharmaceutical and medical devices Agency) for factory auditing for GMP, pharmaceutical manufacturing license, etc...
• Take handover from predecessor.
• Handle related documents.
• Other detail will be discussed in the interview.

• Qualification of pharmacist.
• 7 years experienced in QA Dept in pharmaceutical manufacturing company.
• Good at English.
• Good communication and negotiation skills.
• Exhibit good knowledge of Microsoft Office, Excel.
• Management skills.
• Able to work under high pressure.

*Preferable:

• Experience in corresponding with factory auditing for pharmaceutical manufacturing license is a BIG PLUS.
• [Allowance] Seperately payment for registering Pharmacist certificates at Drug Administration
• Company pick-up bus from HCMC.
• Working time: 8:00 ~ 17:00 (Mon - Fri) + 8:00 ~ 17:00 (2 Saturday/month).