Jesmond Siew

Project Manager at Haw Par Corporation Limited
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Contact Information
us****@****om
(386) 825-5501
Location
Singapore, Singapore, SG

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Experience

    • Singapore
    • Health, Wellness & Fitness
    • 1 - 100 Employee
    • Project Manager
      • Jan 2020 - Present

  • Clearlab SG Pte Ltd
    • Central Singapore
    • Manufacturing Manager
      • Dec 2015 - Jan 2020

      • Overall in-charge for manufacturing activities across the business which include production activities, warehouses supply chain, logistic monitoring as well as raw material monitoring • Create and implement best practice manufacturing vision, strategy, policies, processes and procedures to aid and improve business performance • Lead, develop and implement variable cost productivity programmes across all areas of responsibilities • Provide design for manufacturing input at early stages in the new product development process, coordinating with and supporting the new product development team to implement new and revised designs and developing effective processes to ensure manufacturability of product while maintaining quality, safety and environmental standards and achieving cost targets • Provide leadership to departments under control; coach, mentor and develop direct reports and manage a high performing team that delivers continuous improvement, added value and cost reductions • Establish strategy and best practices for staff to ensure achievement of overall business objectives. Work with the Manufacturing team to translate site strategy into specific annual performance goals and departmental objectives including KPIs, and to track them • Ensure strong communication between teams under leadership to facilitate exchange of information and in order to implement change and improvements • Input and hold responsibility for manufacturing budgets • Prepare the annual Manufacturing budget and forecasts and all Capital Expenditure proposals as well as ensuring compliance with legal standards. Manage the budget from identification to completion of projects Show less

    • Switzerland
    • Medical Equipment Manufacturing
    • 700 & Above Employee
    • Senior Validation Engineer
      • Apr 2015 - Dec 2015

      As 3rd parties: • Responsible to qualify the Clean Steam Generation System • Responsible to qualify the WFI Generation System – 6 staged evaporation • Responsible to qualify the RO Pre-treatment & Generation System • Perform capability study on aseptic filling machine • Evaluate and justify Isokinetic Probe location for Grade A environment (Audit Finding) • Evaluate of temperature mapping for finished goods warehouse and incubator As 3rd parties: • Responsible to qualify the Clean Steam Generation System • Responsible to qualify the WFI Generation System – 6 staged evaporation • Responsible to qualify the RO Pre-treatment & Generation System • Perform capability study on aseptic filling machine • Evaluate and justify Isokinetic Probe location for Grade A environment (Audit Finding) • Evaluate of temperature mapping for finished goods warehouse and incubator

    • Assistant Engineering Manager
      • Apr 2011 - Apr 2015

      Tasks and Responsibilities • Fully responsible to monitor and qualify the entire equipment/system of Clearlab SG. • Responsible to create/update the Site Validation Master Plan to fulfill the US FDA, ISO standard. • Fully responsible to create/update the product quality risk management to comply with ISO 14971. • To provide and develop knowledge of validation in order to conduct an in-house training to improve knowledge of validation for all related personnel. • To responsibility of Clearlab calibration system to make sure accuracy of the instruments. • To monitor and ensure that the entire Clearlab production instruments and/or machine which use for production is calibrated in order to make sure accuracy of the instruments and/or machine. • Responsibility to ensure of Clearlab WSH condition in order to reduce the accident rate. • As Clearlab WSH Committee Chairmen which to responsibility to ensure that to meet the government safety requirement. Show less

    • Senior Process Engineer
      • Dec 2008 - Mar 2011

      Tasks and Responsibilities • Responsible to monitor and qualify equipment/system of Clearlab SG. • To prepare and execute all machines, process and material qualification and engineering study in order to comply with all the related regulations such as ISO13485, FDA CFR Part 820 and EU MDD. • To improve process performance in order to sustain product quality and quantity. • To monitor machine performance in order to ensure good product quality and yield results set by management. • Responsible to perform machine upgrading for all the equipment and instruments with business related project. • Fully in-charge in primary packaging output and yield improvement. • Involved in setting up, commissioning and validating the Purified Water system in meeting USP and BP requirements. Show less

    • Medical Equipment Manufacturing
    • 700 & Above Employee
    • Senior Process Engineer
      • Dec 2004 - Dec 2008

      Tasks and Responsibilities • To established and maintain an efficient production process and system. • Provide engineering improvement to production equipment. • Design and write validation protocols and execute change control activities in equipment/systems qualifications (IQ/OQ/PQ). • To improve yield and product quality through 6 sigma and FMEA. • To ensure the rational statistical and quality engineering methods are used to evaluate process capability, acceptance criteria and operation procedures comply with FDA and GMP regulatory. Show less

    • Malaysia
    • Semiconductor Manufacturing
    • 700 & Above Employee
    • Tooling Technician
      • Jul 2000 - Jul 2001

      Tasks and Responsibilities • Fully response in Micro Lead frame Package (MLP) trim and form machine, • Machine trouble shooting, • Implementation of new improvement project, • Taking preventive action to ensure minimum equipment down time, • Tool and Die design, • Machine downtime and cost reduction. Tasks and Responsibilities • Fully response in Micro Lead frame Package (MLP) trim and form machine, • Machine trouble shooting, • Implementation of new improvement project, • Taking preventive action to ensure minimum equipment down time, • Tool and Die design, • Machine downtime and cost reduction.

  • Hitachi Nippon Steel (S) Pte Ltd
    • Manufacturing Technician
    • Manufacturing Technician
      • Dec 1997 - Feb 1999

      Tasks and Responsibilities • Trouble shoot and report any equipment related problem, • Taking preventive to ensure minimums down time, • Promotes team work within the department, • Train and imparts knowledge to manufacturing specialist. Tasks and Responsibilities • Trouble shoot and report any equipment related problem, • Taking preventive to ensure minimums down time, • Promotes team work within the department, • Train and imparts knowledge to manufacturing specialist.

Education

  • Northumbria University
    Master's Degree, Manufacturing
    2002 - 2003
  • DPS Engineering
    Certificate in Pharmaceutical Manufacturing, Validation
    2010 - 2010
  • Northumbria University
    Bachelor's Degree, Mechanical Design
    2000 - 2002

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