Job Description

How Will You Make an Impact?

Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $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, improving patient diagnostics and therapies or increasing productivity in their laboratories, 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 and Patheon. For more information, please visit

When you\'re part of the team at Thermo Fisher Scientific, you\'ll do important work. Surrounded by collaborative colleagues, you\'ll have the support and opportunities that only a global leader can give you. Our respected, growing organization has an outstanding strategy for the near term and beyond. Take your place on our strong team, and help us make significant contributions to the world.

Job Purpose:

Perform material inspections, environmental monitoring, batch record reviews and finished product release in accordance to established quality systems that meet ISO13485 and 21-CFR-820 requirements

Essential duties and responsibilities:

• Perform inspection on product to ensure compliance with quality specifications, particularly ISO13485:2003 and 21-CFR-820.
• Perform manufacturing batch record and documentation review with excellent attention to details for completeness and accuracy prior to product release and/or closure.
• Communicate effectively and coordinate task with Manufacturing and Quality Control to ensure timely release of products.
• Perform environmental monitoring, measurement and publish test report.
• Perform physical Nonconforming Material segregation and disposition per approved instructions.
• Perform inventory transaction in JDE as part of quality inspection and product release process.
• Maintain filling system for outgoing inspection reports.
• Assist new colleagues on their On-the-Job (OJT) by acting as their buddy as well as coaching the junior Technician in their areas of work.
• Provide feedback and give suggestion to work process improvement.
• Track and trend functional metrics.
• Perform QA updates at daily Tier meeting.

Minimum requirement:

• Minimum ITE or equivalent
• Minimum 5-year QA/QC experience in clean room environment, preferably in semiconductor / pharmaceutical/ biotech industries.
• Microsoft office skills especially in Excel with good analytical skills.
• Meticulous and attention to details with good troubleshooting ability.

Preferred requirement:

• Data entry skills and familiarity with inventory management systems.
• Good communication and teamwork skills.

Additional Information:

• Transport is provided at certain locations around Singapore.

Working location: Gul Circle

Working hours: Mondays to Fridays, 8am to 5.15pm

Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain . As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

Job Category

Manufacturing & Production, Operations, Quality

Thermo Fisher Scientific

is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

Thermo Fisher Scientific