Do you want to help ensure the quality of systems and processes at a leading pharmaceutical company? You will support the engineering team in qualifying equipment throughout its entire lifecycle. * Reviewing and approving qualification and validation documents (SOPs, URS, risk assessments, test plans, scripts, change controls, CAPAs, etc.) * Supporting engineering teams with the introduction of new or updated systems and processes * Experience with change control management (preferably using TrackWise) is an asset.
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