Job Description

Work Schedule

Environmental Conditions

We are seeking an exceptionally dedicated individual to join our team at Fisher Clinical Services Japan K.K. This is an outstanding opportunity to be part of a world-class organization dedicated to maintaining the highest standards in the handling and management of investigational drugs.

Main Responsibilities:

• Complete all processes in strict accordance with established procedures and cGMP standards.
• Ensure that facilities and workspaces are kept clean and tidy.
• Verify that equipment and tools within the work area are maintained and functioning flawlessly.
• Complete regular reports related to the work area as required by supervisors or clients.
• Maintain accurate documentation of all processes completed.

Receiving:

• Verify received shipments against documentation and system records, and inspect all incoming drugs.
• Store materials under appropriate temperature conditions and locations.
• Complete documentation and update computer systems accurately and appropriately.

Disposal:

• Process orders timely and accurately.
• Package and ship investigational materials accurately and appropriately.
• Ensure compliance with project instructions.
• Verify that complete and accurate shipping information is provided to carriers.
• Document tasks correctly and input data into systems accurately and appropriately.

Shipping:

• Verify the accuracy of picked drug supplies against customer orders and shipping documents.
• Conduct in-process checks for just-in-time labeling.

Returns and Disposal:

• Verify received shipments against documentation and system records.
• Retrieve and package all materials from inventory according to customer instructions.
• Arrange appropriate shipping and/or destruction of materials according to customer instructions.
• Complete documentation and update computer systems accurately and appropriately.

Qualifications:

• High school diploma or equivalent.
• At least 3 years of experience in logistics or warehouse-related work.
• Experience working in a GMP/QMS environment is preferred.
• Practical knowledge of Microsoft Office (MS Word, Excel, PowerPoint, Outlook).
• Ability to read and write in English and basic conversational skills.

Join us in our ambitious mission to ensure flawless handling and management of investigational drugs and contribute to our world-class standards!

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