Industrial Engineer - #1096663

Quasar Medical (Singapore) Pte Ltd


Date: 4 days ago
District: Sembawang
Salary: $4,500 - $6,000 / month
Contract type: Full time
Work schedule: Full day
Quasar Medical (Singapore) Pte Ltd

Essential Duties and Responsibilities:

Include the following. Other duties may be assigned.

·        Establish a system for systematic audit of established manufacturing methods and time standards, including timely closure for any gaps identified.

·        Engagement with relevant functions in the resolution of manufacturing issues associated with manufacturing methods and time standards, including timely closure for any gaps identified.

·        Develop, prepare and present performance reports for manufacturing operations review and drive closure to issues identified for further improvement through analysis and engagement with responsible functions.

·        Design and present layout of manufacturing processes, equipment and materials to optimize space and improvement in work efficiency; using lean methodology and concepts to reduce waste.

·        Engagement with all relevant functions to support layout request in the company, ensuring that layout meets company codes and standards.

·        Ensure engineering master data (primarily MM, Routing, Work Centres, and BOM) are set-up and maintain correctly and updated in a timely manner.

·        Participation in 6 sigma projects, Kaizen events, and continual improvement projects from time-to-time.

·        To assist in facility related matters in his secondary role.

·        Other assignments to be given by the Facility Manager from time-to-time.

 

Education/Experience and Qualifications:

  • Degree or diploma in mechanical, electrical engineering, or a related technical field, with 3-5 years of experience in a high-volume production environment; experience in medical device manufacturing is preferred.

  • Experience in writing protocols for validations and qualifications is a plus

  • Proficiency in CAD/CAM software (e.g., SolidWorks or Pro/ENGINEER) is a plus

  • Knowledge of industry standards such as GMP, ISO 9001, and ISO 13485 is preferred.

  • Understanding of cleanroom requirements for manufacturing is beneficial.

  • Familiarity with facility equipment and systems is a plus.

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