To carry-out pre and post inspection, which include inspection on mould after mould change and mould condition prior to use, reinforcement arrangement, accessories and cast-in item, dimensional and appearance condition based on issued drawing.
Ensure thorough knowledge of ResMed’s Quality system to work within established policies and procedures, compliance with GMP, regulatory requirements and other business systems.
Participate in the Margin team’s full software development lifecycle, from requirements analysis and test planning to execution, defect tracking, product delivery, and maintenance, with a strong focus on Java / Rust-based trading and risk systems.
Diploma or Degree in Food Science, Food Technology, Microbiology, or a related field, with WSQ Food Safety Course Level 3 (eligible to register as a Food Hygiene Officer with SFA).
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
Reviews, analyzes, and makes recommendations on investigations, while identifying enhancements to ensure cases meet or exceed closure and quality metrics