Job Description

How Will You Make an Impact? Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team of more than 100,000 colleagues delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD. For more information, please visit www.thermofisher.com What will you do?

• Inspect incoming raw materials and components to ensure compliance with product specifications, particularly ISO13485 and 21 CFR 820.
• Perform manufacturing batch record and documentation review for completeness and accuracy prior to product release and/or closure.
• Perform environmental monitoring, measurement and publish test report.
• Performing physical non-conforming material segregation and disposition per approved instructions.
• Perform inventory transactions in JDE as part of quality inspection and product release process.
• Maintain filing system for the incoming inspection reports.

• Minimum ITE or equivalent and able to perform.

• 1 - 3 years QA experience in clean room environment, preferably in semiconductor / pharmaceutical / biotech industries. Fresh graduates with NTC in Chemical Process Technology can apply.

• Ability to read, interpret and understand technical and non-technical supplier control documents including product drawings, specifications.
• Able to work 12-hour permanent day shift.

• Transport is provided at certain locations around Singapore.