Experience in validation of analytical instrument systems (e.g. benchtop analytical systems - spectroscopy, chromatography, protein analyzers, next gen sequencers, PCRs etc.)
Author validation life cycle documents for client’s review and approval
Dafted documents for review and request approval workflows to Doc Control
Execute approved protocols in GxP facility
Understand SDLC process and SDLC methodology such as agile etc.
Work with global team in delivering validation project deliverables
Experience in process compliance and interface with Quality Assurance change control area
7+ years’ experience in a Validation/ Quality assurance / control role, preferably in the pharmaceutical /Life sciences industry preferred.
Please submit for more detailed JD.
Job Type: Full-time
Pay: $40.02 - $48.20 per hour
Work Location: In perso

Please refer the Job description for details