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This position works out of our Tuas location in the Abbott Manufacturing Site.Comply to all policies and standards. Develop, execute and review validation protocols and related documentation in accordance with Abbott procedures and policies. Lead Failure Mode Effects Analysis (FMEA) for new equipment installations or changes. Manages site Validation Review processes (VRB), review and approve site change controls (plant and laboratories related) and validation change requests. Perform root cause analysis and identify corrective and preventive actions in addressing quality events Support resolution of validation events and escalate concerns in a timely manner. Support in equipment and process walkdowns ...
About the Role
The Opportunity
This position works out of our Tuas location in the Abbott Manufacturing Site.
As the Quality Engineer (Validation), you’ll have the chance to ensure that change control and validation activities are executed in a timely manner.
What You’ll Work On
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