How Will You Make an Impact? Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $25 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 75,000 colleagues...

-Inspect incoming raw materials and components to ensure compliance with quality specifications, particularly ISO 13485 and FDA 21 CFR part 820. -Perform inspection, manufacturing batch record and documentation review for completeness and accuracy prior to product release and/or closure -Perform physical Nonconforming Material segregation and disposition per approved instructions. -Perform inventory transactions in JDE as part of quality inspection and product release process. -Maintain filing s...

How Will You Make an Impact? Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $25 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 75,000 colleagues...

Job Purpose: Supervise and co-ordinate all production activities to meet manufacturing goals through efficient use of resources (i.e. manpower, materials, machines and methodologies) in a safe and healthy working environment. Essential Duties & Responsibilities include the following : Other duties may be assigned. Act as main co-coordinator for all the other Manufacturing Engineers in meeting all manufacturing goals and key performance indices. May need to perform shift duties to support pro...

Office hours: Monday to Friday, 8am - 515pm Location: Gul Circle (2 way company bus transport available from selected islandwide MRT stations) Reporting to: Staff Engineer, Manufacturing Responsibilities: - Support New Product Introduction (NPI) and product transfers from R&D and Contract Manufacturer (CM). - Provide Product Engineering support such as second level failure analysis, and cost reduction through value engineering activity. - Provide Sustaining Engineering support such as improv...

Setting up and operating a variety of equipment used in the production of GeneChip® probe arrays. Ensure that the best quality and output of products are achieved. Job Descriptions:   Ensure work performed adhere to ISO 13485:2003 and 21- CFR – 820 requirements. Non-compliance to operational procedures by MAs are to be reported to MEs immediately. Perform routine and repetitious work within narrowly defined parameters. Operate on the tools with discipline and maintain good housekeeping prac...

Job Responsibilities: Ensure work performed adhere to ISO 13485:2003 and 21-CFR-820 requirements. Non-compliance to operational procedures by MAs are to be reported to MEs immediately. Perform routine and repetitious work within narrowly defined parameters. Operate on the tools with discipline and maintain good housekeeping practices in the clean-room environment. Cultivate good working habits and inform the Technical Specialist of any problem encountered with the tool or product. Inform MEs imm...

Job Purpose Supervise and co-ordinate all production activities to meet manufacturing goals through efficient use of resources (i.e. manpower, materials, machines and methodologies) in a safe and healthy working environment. Essential Duties & Responsibilities Act as main co-coordinator for all the other Manufacturing Engineers in meeting all manufacturing goals and key performance indices. May need to perform shift duties to support production. May also need to supervise a team comprising M...

Roles & Responsibilities: Inspect incoming raw materials and components to ensure compliance with quality 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. Manage calibration program to support measurement instruments used for product release and environmental monitoring. Perform environmental monitoring, measurement and publish test report. Performing physic...

How Will You Make an Impact? Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $25 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 75,000 colleagues...

How Will You Make an Impact?   Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $25 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 75,000 col...

Ensure work performed adhere to ISO 13485:2003 and 21- CFR – 820 requirements. Non-compliance to operational procedures by MAs are to be reported to MEs immediately. Perform routine and repetitious work within narrowly defined parameters. Operate on the tools with discipline and maintain good housekeeping practices in the clean-room environment. Cultivate good working habits and inform the Technical Specialist of any problem encountered with the tool or product. Inform MEs immediately in the eve...

1. Daily operation of analytical tools 2. Basic data analysis of testing results...

1. Daily operation of analytical tools 2. Basic data analysis of testing results...

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Job Title: IT Site Support Analyst Office location: Joo Koon (Walking distance to MRT station) Reporting to: IT Manager  Work hours: Mon-Fri, 8am to 515pm   When you join us at Thermo Fisher Scientific, you’ll be part of a smart, driven team that shares your passion for exploration and discovery. With revenues of more than $24 billion and the largest investment in R&D in the industry, we give our people the resources and opportunities to make significant contributions to the world....

Work Hours: Mon-Fri, 8am - 515pm Location: Joo Koon (5 mins walk from MRT station)  Reporting to: Senior Manager, Procurement  Responsibilities: Review and analyze materials requirements for production and execute the necessary actions such as generating Purchase Order, scheduling and re-scheduling of material based on MRP requirement. Manage supplier base to achieve delivery performance and negotiate with supplier to ensure optimum cost competitiveness. To provide guidance to Junior B...

Work Hours: Mon-Fri, 8am - 515pm  Location: Near Joo Koon MRT station, walking distance  Reporting to: Director, Facilities & EHS / Sustainability  Position Summary: This position will be primarily responsible for infrastructure and facilities at the Single Use Technology (SUT) bioproduction manufacturing site planned at 3A Joo Koon Circle. The manager shall anticipate, strategize, plan, budget, and schedule facility maintenance and repair, modifications, including estima...

Operating hours: Mon-Fri, 8am to 515pm  Location: Gul Circle (2-way company shuttle bus available islandwide)  Reporting to: Senior Manager, Quality Control Responsibilities: The QA/QC LIMS Engineer performs the major functions listed below.  The QA/QC LIMS Engineer will be responsible for implementing and supporting the daily needs of QA/QC testing activities. Establish and maintain relationships with colleagues and peers as well as performing necessary administrative duties as r...

Operating Hours: Mon-Fri, 8am - 515pm  Location: Gul Circle (2-way company shuttle bus islandwide available)  Reporting to: Senior Manager, Quality Control Responsibilities: Review and approves validation protocols for product and process changes. Review and approve revision changes to DOPs, manufacturing process, components, software and labeling. Ensure failure investigations are performed and well documented for non-conforming materials and products. Establish and maintain database ...