職責(zé)描述：
1. Experienced in GMP quality management improvement
2. Able to handle regulatory inspections from FDA, EMA, NMPA etc GMP audits from clients as well as internal quality assurance unit
3. Lead GMP investigations provide guidance/direction to the team finvestigations
4. Play a role in critical majquality related issue detection associated trouble-shooting investigation.
5. Involve to assist solving key quality issues as requested by the team.
6. Experienced in cross-functional communication.
任職要求：
Qualification
1. Master degree equivalent in Analytical other directly related science discipline with pharmaceutical industry experience of no less than 8 - 10 years in quality related position.
2. Proven good track record of accomplishments in the quality management area
3. Fluental English communication skill.