Responsibilities

1 Distribute and archive newly updated internal GMP document and local pharmaceutical regulatries
2 Update SOPs within responsible area
3 Assist and participate in SOP management
4 Responsible in management of other GMP related document, such as Site Master File and Registration Document
5 Stimulate awareness within plant of updated requirements for prompt and positive action to assure comliance
6 Develop training programs within responsible area

Qualifications

1 With +5 years experience in Pharmaceutical quality assurance
2 Progressive knowledge of cGMP requirements
3 Strong interpersonal skills
4 Effective organization and time management skills
5 Written and verbal communication skills both in Mandarin and English
6 Excellent abilities in generating and/or maintain databasees and presentations