Manufacturing Engineer

4 days ago

Chon Buri, Chon Buri, Thailand Quasar Medical (Thailand) Co., Ltd. Full time

Quasar's Manufacturing Engineering Team has the responsibility of working with cross-functional teams comprising of Quality, Production, Supply Chain and Program Departments to achieve organization's goals. Manufacturing Engineers own the processes for one or more product lines and are responsible for implementing Continuous Improvement Projects (CIPs), working together with RFQ Engineer to provide accurate Technical Costing and building samples for new projects. Manufacturing Engineers works closely with Advanced Engineering Team and New Product Introduction (NPI) Team to execute a clean handover of projects from NPI to Mass Production.

Responsibilities:

  • Health & Safety: Ensure that all Health, Safety and Environmental requirements are fulfilled for the manufacturing process.
  • Quality: Drive Engineering solutions to ensure Right First-Time principles, driving yield improvements, complaint reductions, supporting the CAPA process, and audit prep activities.
  • Continuous Improvement: Own the manufacturing process, work with key business stakeholders and operations teams to assess process capabilities, improve process efficiency, reduce cycle time.
  • Service: Drives a culture of Exceptional Customer Experience (ECE) for both the Internal and External customers, by ensuring that projects and commitments and continually being met or exceeded.
  • New opportunity sample build: Conduct the new opportunity sample build, by ensuring that product and commitments being met or showing manufacture capability to customer.
  • Responsible for managing the overall process performance through the appropriate use of Lean Manufacturing tools and techniques (TPM etc.).
  • Responsible for preparing validation protocol of OQ&PQ/PV for additional TJ/equipment, and process period to mass production.
  • Develop and manage SOPs/manufacturing standards/operations standard work as required in compliance with engineering change control process (ECO).
  • Investigating in state-of-the-art process technologies and evaluating potential competitive advantage and the cost-benefit of introduction.
  • Maintain high quality / compliance standards in line with Medical Devices manufacturing requirements.
  • Drive MP product to keep stably high manufacturing yield.
  • Manage a variable workload to meet operational requirements.

Qualification:

  • College degree or above, major in engineering, mechanical, electronic, or equivalent.
  • Above 5 years' + related working experience. Medical product development/manufacturing will be preferred.
  • Experience in failure analysis, root cause analysis, and corrective action implementation.
  • Demonstrate a dynamic, motivated & flexible approach to work with results-oriented attitude.
  • Demonstrate a practical understanding of Lean Manufacturing principles and statistics.
  • Excellent communication, planning and organizational skills.
  • Fluent English skills.
  • Skillful AutoCAD and MS office (SolidWorks/Pro-E skills is an advantage)
  • Knowledge of ISO & FDA compliance is an advantage.

Working Conditions

  • Working Days: Monday to Friday
  • Working Hours: 08:30 – 17:30
  • Uniform: Not required
  • Company Transportation: Not provided
  • Canteen: Available

Benefits

  • Fixed Bonus
  • Variable Bonus
  • Group Insurance
  • Provident Fund

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