Be responsible for planning, implementation and daily handlings of shipment orders to ensure clinical trial materials are well- supplied in accordance with the cGMP standards.
Perform all processes in accordance to established procedures and cGMP standards Support the activities of planning, implementing, motivating, co-monitoring, and tracking study documents and tracking tools Coordinate to ensure the shipment orders processing in a timely and accurate manner in accordance with cGMP standards Confirmation of previously entered data and completion of data entry Complete regular reports (as required by Management or client) pertaining to relevant work areas Support PM to update contact listings, update checklist, generate and compile reports as requested. Other job assigned by supervisor
Education: College diploma above. Pharmaceutical or biological preferred. Vocational diploma
will be considered if with satisfactory working experience.
Experience: Rich relevant working experience. Experience in freight operation, logistics
management or international trade..
Knowledge: Good command of English (CET4 or CET6 preferred). Good command of
computer skills (MS Office). Logistics, international trade.
Competency: Customer-oriented. Details-oriented. Teamwork. Ability to work under pressure.
Work Schedule: 08:30 AM TO 05:30 PM core hours, additional hours as required.
1-2 yrs of working experience. Good command of English. Teamwork spirit.
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