What We Can Offer
In general charge of deviation handling, CAPA, change control
Review and periodically report on quality assurance activities
Develop quality system processes. Document system management
Planning of internal inspections - supplier inspections
Make a GMP training plan
Do some quality system management work with authorization from the QA Manager
Responsible, complete the work assigned from the room manager
Report the work to the direct manager
Confidentiality of information according to the regulations of the company.
Bachelor degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Engineering
PROFESSIONAL KNOWLEDGE & SKILLS:
Minimum 4 years of experience in pharmaceutical factory.
Ability to analyze and solve problems
Ability to work under pressure
Understand the systematic process of GMP-WHO, GMP-EU in the pharmaceutical industry.
English : Listen, speak, translate documents well
Microsoft Excel/Word, Autocad
Be careful, honest.
Ability to interact with colleagues at all levels throughout the company.
Support other departments at work