Coordinate with procurement and suppliers to ensure all documentation aligns with contractual, sustainability and ISCC requirements.
Prepare customs clearance documentation for import shipments and maintain the inbound feedstock master data for audit traceability.
Execute MPOB feedstock purchase transactions and ensure all SIMS entries for purchases and movements (to Storage/Plant) are completed within 48 hours.
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Manage Windows 10 & 11, MS Office Applications, network connections, printer mapping etc.
Manage email message configuration and troubleshooting issues for Outlook.
Must be able to troubleshoot laptop or PC problems down to the board level, set up peripherals, connect devices to the network, and install/replace various hardware components, hard drives, etc.
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Performs and documents initial reportability decisions on complaints in accordance with regulations (US FDA) and international regulations (MEDDEV Vigilance, Health Canada, and others as applicable) and company procedures; Elevate complaints that require additional review for regulatory reporting.
Verify that the correct number of complaints have been opened to address all of the issues identified in the complaint description. If required, generate additional complaint records to document all of the issues listed in the complaint description.
Ensure that all complaints requiring customer responses are properly addressed, as assigned; drafts and documents the response in the complaint file.
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Collaboration: You won’t be alone! Work closely with production teams, engineers, and supervisors to enhance product quality. Your insights will shape our processes.
Continuous Improvement: Be at the forefront of innovation. Help create new samples for product development. Your ideas matter!
Detective Mode: Spot unusual activities and report them promptly. You’re our quality detective!
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Conduct evaluation, analysis and report on product application.
Work closely with product development team and technical solution team in achieving their key objective on project by providing application support and knowledge sharing.
Work closely with technical solution team and sales team to recommend and provide product samples for events and exhibitions.
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Performs and documents initial reportability decisions on complaints in accordance with regulations (US FDA) and international regulations (MEDDEV Vigilance, Health Canada, and others as applicable) and company procedures; Elevate complaints that require additional review for regulatory reporting.
Verify that the correct number of complaints have been opened to address all of the issues identified in the complaint description. If required, generate additional complaint records to document all of the issues listed in the complaint description.
Ensure that all complaints requiring customer responses are properly addressed, as assigned; drafts and documents the response in the complaint file.
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