Senior Planner

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Quasar, a global B2B medical device manufacturer is looking to hire Senior Planner, who will join our Operation Department at Singapore.  This position will report to Senior Planning Supervisor

The planner is responsible to ensure the planning for all materials and supplies to meet the operational needs of Quasar Singapore.  This position is responsible for developing and maintaining valid production schedules from the demand forecast to meet customer requirements while utilizing resources efficiently. It will require close communications with process engineering, purchasing, production, quality, customers and suppliers.

  • Participate in the preparation of the master production schedule.
  • Execute the material ordering and planning to meet the master schedule and site revenue.
  • Prepare reports and inform management team of scheduling and materials problems as they arise.
  • Develop and implement systems that ensure a smooth and reliable flow of materials from vendors through the production cycle.
  • Ensure appropriate inventory levels are maintained including the stock room, WIP, and lab supplies.
  • Size up Materials Clear to build and provide supply commit to Customer Service base on Materials and Capacity.
  • KPI includes Revenue, Inventory Days of Supply, Aging Materials Control and Customer OTD.
  • Support Monthly report of MOR.
  • Support cost reduction initiatives and Assurance of Supply to meet cost and supply need.
  • Back up customer service or buyer during leave period.
  • Maintain and comply with ISO13485, GMP and FDA regulations.
  • Other duties may be assigned.


  • Management or technical diploma degree, BS preferred with 5 to 10 years of planning experience in a manufacturing environment, preferably in Medical Device Manufacturing.
  • Excellent Communication Skills
  • Knowledge of GMP, JIT, SPC, TQC concepts and procedures required
  • Familiar with LEAN and Six Sigma methodologies
  • Working knowledge of ERP systems
  • Computer literacy required.  Familiar with Microsoft office software.
  • Knowledgeable in writing procedures and GMP requirements
  • Knowledge of GMPs, ISO 9001, ISO13485 and the Medical Device Directives.
  • Work Environment While performing the duties of this Job, the employee is frequently exposed to moving mechanical parts. The noise level in the work environment is usually moderate.


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