Perform fuel handling operations, including fuel quality checks, fuel loading/unloading, refuelling activities, and maintaining accurate operational records.
Perform fuel handling operations, including fuel quality checks, fuel loading/unloading, refuelling activities, and maintaining accurate operational records.
Perform fuel handling operations, including fuel quality checks, fuel loading/unloading, refuelling activities, and maintaining accurate operational records.
Location: Gul Circle (Pick up @ Choa Chu Kang / Jurong East / Woodlands)Duration: 6 MonthsSalary: $2300Working days and hours:- 8am to 5.15pm, Monday to Friday (with 45mins lunch break, 15mins tea break)Job Description:- Perform QC testing and review of QC data to support the timely release of GeneChip arrays.- Provide data trending and assist team leads in troubleshooting failure analysis. Technical duties- Perform QC testing of GeneChip products to ensure compliance with quality specifications, particularly in compliance with ISO 13485, MDSAP and 21- CFR – 820 requirements.- Perform target preparation for Cytoscan and Axiom.- Perform review and disposition of QC batch records for release to QA.- Perform preventive maintenance for QC equipment.- Schedule QC testing and target preparation- Support and conduct in lab investigation relating to product failures & participate in the implementation of corrective actions as necessary.- Support and conduct experiment /analysis to support new product release & enhancement of test methods.- Trending & monitoring of QC test data to support failure analysis, investigation & troubleshooting.- Perform QC updates at daily Tier 1 meeting.- Support FQC Supervisor in accomplishing tasks as assigned. Administrative duties- Ensure controlled documents to support QC operation are properly maintained and readily available.- Provide training to other junior employees and QC staff as required.Job Requirements:- Min Diploma in Biomedical Engineering, Biomedical Science, Biotechnology or any relevant field
Location: Gul Circle (Pick up @ Choa Chu Kang / Jurong East / Woodlands)Duration: 6 MonthsSalary: $2300Working days and hours:- 8am to 5.15pm, Monday to Friday (with 45mins lunch break, 15mins tea break)Job Description:- Perform QC testing and review of QC data to support the timely release of GeneChip arrays.- Provide data trending and assist team leads in troubleshooting failure analysis. Technical duties- Perform QC testing of GeneChip products to ensure compliance with quality specifications, particularly in compliance with ISO 13485, MDSAP and 21- CFR – 820 requirements.- Perform target preparation for Cytoscan and Axiom.- Perform review and disposition of QC batch records for release to QA.- Perform preventive maintenance for QC equipment.- Schedule QC testing and target preparation- Support and conduct in lab investigation relating to product failures & participate in the implementation of corrective actions as necessary.- Support and conduct experiment /analysis to support new product release & enhancement of test methods.- Trending & monitoring of QC test data to support failure analysis, investigation & troubleshooting.- Perform QC updates at daily Tier 1 meeting.- Support FQC Supervisor in accomplishing tasks as assigned. Administrative duties- Ensure controlled documents to support QC operation are properly maintained and readily available.- Provide training to other junior employees and QC staff as required.Job Requirements:- Min Diploma in Biomedical Engineering, Biomedical Science, Biotechnology or any relevant field
Location: Gul Circle (Pick up @ Choa Chu Kang / Jurong East / Woodlands)Duration: 6 MonthsSalary: $2300Working days and hours:- 8am to 5.15pm, Monday to Friday (with 45mins lunch break, 15mins tea break)Job Description:- Perform QC testing and review of QC data to support the timely release of GeneChip arrays.- Provide data trending and assist team leads in troubleshooting failure analysis. Technical duties- Perform QC testing of GeneChip products to ensure compliance with quality specifications, particularly in compliance with ISO 13485, MDSAP and 21- CFR – 820 requirements.- Perform target preparation for Cytoscan and Axiom.- Perform review and disposition of QC batch records for release to QA.- Perform preventive maintenance for QC equipment.- Schedule QC testing and target preparation- Support and conduct in lab investigation relating to product failures & participate in the implementation of corrective actions as necessary.- Support and conduct experiment /analysis to support new product release & enhancement of test methods.- Trending & monitoring of QC test data to support failure analysis, investigation & troubleshooting.- Perform QC updates at daily Tier 1 meeting.- Support FQC Supervisor in accomplishing tasks as assigned. Administrative duties- Ensure controlled documents to support QC operation are properly maintained and readily available.- Provide training to other junior employees and QC staff as required.Job Requirements:- Min Diploma in Biomedical Engineering, Biomedical Science, Biotechnology or any relevant field