Job Description
Description
About the role:
As a Manufacturing Associate I, you will perform and document daily manufacturing operations according to SOPs in a cGMP environment. You will operate biologics production equipment (bioreactors, filtration units, chromatography systems and fixed/portable vessels) and will execute validation protocols. You will report to the Manufacturing Supervisor.
This is a day shift role with a rotating schedule. The working hours are from 5:45 AM to 6:15 PM.
How you will contribute:
Perform dispensing, labeling, and transferring/staging of raw materials and parts.
Will assemble/disassemble, clean, and sterilize components, parts, and equipment.
Maintain equipment, area, and cleaning logbooks.
With general management or guidance will assemble and operate biologics production equipment, such a bioreactors, filtration units, chromatography systems an...
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