Job Description

Its an American pharmaceutical company headquartered in North Chicago, Illinois. It is ranked sixth on the list of largest biomedical companies by revenue.Validation engineers manage, inspect, calibrate, test and modify the instrumentation, equipment, mechanics and procedures used in manufacturing. A critical aspect of their job is documenting this process so there is evidence that systems are operating safely and efficiently.Validation engineers can be found in a range of industries, including aerospace, automotive, computer software and pharmaceuticals. This means the role varies depending on your industry and specialism.Typical duties include: following master validation plans. calibrating and testing equipment, and directing this work. documenting results. Building knowledge of products, equipment and systems.preparing compliance reports. making sure work is done within safety guidelines and legislationdeveloping documentation to support the testing process. resolving testing problems. making adjustments or improvements to equipment and processes based on test results.investigating equipment failures.creating databases to track validation activities.interpreting customer requirements.developing validation schedules.conducting training and overseeing the work of validation technicians.maintaining instrumentation and equipment. keeping up to date on industry standards and regulations. Staff need to work on shiftsJob Type: Contract, Contract length: 12 monthsSchedule: Shift systemExperience: CQV: 1 year (Preferred) Work Location: In personApplication InstructionsPlease apply for this position by submitting your text CV using InternSG.
Kindly note that only shortlisted candidates will be notified.

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