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Major Tasks and Responsibilities:
1.After 3 weeks of training, be able to perform daily analytical work under the guidance of skilled analyst.
2.Translate some technical documents and CMS.
3.After 5 weeks of training, familiar with the related content of method validation, method verification and method transfer, then be able to draft related protocol.
4.Calculate QC workload and cost for the introduced new products.
Requirement:
1.University degree or above, major in pharmaceutical or related subjects.
2.Good English command & Good Computer skill.
3.Team work spirit, good communication and logical analysis.