Ensure that Global DC’s have sufficient Days on Hand of Finished Goods inventory at all times
Plan and execute on Finished Goods distribution strategy to replenish stock levels at the DC’s
Maintain a positive working relationship with DC Managers, Production, Planning, & Warehouse/Logistics to ensure a streamlined flow of communication and timely inventory receipts
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Supports, troubleshoots and maintains Corporate and Manufacturing systems (i.e. deploying enhancements/bug fixes).
Collaborate with team members (project manager, software developers, systems and network engineer) in a fast-paced environment to meet project milestones.
Systems validation and documentation meet predetermined guidelines for compliance.
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Assist Quality Manager on the quality assurance and product quality
Supports product manufacturing through the application of quality engineering tools
Assure conformance of systems and processes during manufacture, and quality control operations with respect to internal procedures, Quality System Regulations (FDA CFR 21 820), ISO 13485, Canadian Medical Device Requirements (CMDR) and other applicable international standards and regulations
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Develop project plans, timelines, and budgets for the projects.
Coordinate resources, tasks, and activities to ensure timely and efficient project execution.
Collaborate with cross functional teams including engineers, planner, production, buyer to ensure effective communication, coordination, and collaboration throughout the project lifecycle.
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Responsible for quality compliance duties relating to customer complaints, including but not limited to preliminary classification of complaints, customer and product follow ups, maintaining investigation records and all other supporting documentations, and assign additional actions as necessary to close complaint.
Ensures complaints are processed thoroughly and timely in compliance with departmental procedures and metrics.
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Responsible for driving the growth and adoption of Masimo's Automation, Connectivity, and Capital Equipment solutions across Singapore.
Develop, maintain, and execute strategic business development plans to identify, qualify, and convert automation and capital equipment opportunities.
Build and manage a sustainable sales pipeline, including new installations, system upgrades, technology refreshes, workflow optimization projects, and account expansion initiatives.
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Comply with the procedures defined in the Quality System, Company Policies and Malaysian Labor Law.
Supervise hiring, training and performance of associates and leads.
Work together with Quality and Process engineering department to clearly document steps and acceptance criteria of the product assembly in the appropriate manufacturing documentation (MAP and AP’s) and Visual aids.
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The physical demands of the position described herein are essential functions of the job and employees must be able to successfully perform these tasks for extended periods.
Ensure the Company’s quality system is effectively implemented and supported in the Malaysia facility.
Implement and maintain effective statistical process controls and other statistical techniques to ensure manufacturing output is in control and monitored.
Responsible for the coordination of Incoming, In-Process, and/or Finished Goods Acceptance Testing;
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Plan, conduct, and document QMS internal audits in accordance with established audit schedules and company procedures.
Evaluate compliance with applicable regulations, standards, and quality system requirements, including ISO 13485, 21 CFR Part 820, EU MDR 2017/745 and other relevant global regulatory requirements.
Evaluate the effectiveness of quality system processes and ensure they are adequately documented, implemented, and maintained.
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The physical demands of the position described herein are essential functions of the job and employees must be able to successfully perform these tasks for extended periods. Reasonable accommodations may be made for those individuals with real or perceived disabilities to perform the essential functions of the job described.
Assist Quality Manager on the quality assurance and product quality
Supports product manufacturing through the application of quality engineering tools
Assure conformance of systems and processes during manufacture, and quality control operations with respect to internal procedures, Quality System Regulations (FDA CFR 21 820), ISO 13485, Canadian Medical Device Requirements (CMDR) and other applicable international standards and regulations
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Request and /or generate production orders for assemblies and sub-assemblies according to the build plan requirement.
Make the analysis of the build plan requirement vs current capacity, in order to escalate if there is any constraint.
Supports the forecasting process to define the overall demand plan. Ensures that the agreed upon demand plan is loaded in Rapid Response and other production planning tools are developed and maintained to support the timely production of product to meet customer requirements and maintain the desired amount of inventory.
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Ensure Molding production equipment and machinery in the plant achieves minimum machine downtime and obtains minimum NCR.
Provide engineering support to Production, Engineering and QC in terms of process improvement, repairs, troubleshooting of automation and control system, calibration and process validation.
To carry out the change request and evaluate the change effects on validated process.
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Lead by example in customer service, greet customer and give assistance and make sure standards are followed to reflect a strong image for our brands and company.
Reviews and analyses sales figures to identify opportunities to develop and drive sales performance at department and BU level.
Challenges the team to improve performance compared to business and shape of chain using relevant retail metrics.
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