Sr Manufacturing Engineer (Medical)

Jabil Circuit (Singapore) Pte Ltd; Singapore; On-site; SGD 60,000 - 90,000; Full time

Job summary

Jabil Circuit (Singapore) Pte Ltd. seeks a Manufacturing Engineer III to plan, design, implement, and manage integrated production and service delivery systems ensuring performance, reliability, maintainability, and cost control at the site.

The role emphasizes profitability, effectiveness, adaptability, responsiveness, quality, and continuous improvement across product life cycles. Candidates should demonstrate strong industrial engineering skills and cross-functional collaboration.

Qualifications

• Broad range of industrial engineering tools application.
• Understanding of site facilities and how they tie to company strategy.
• Strong financial and analytical ability.
• Proven change management and cost reduction experience.
• Strong communication skills.

Responsibilities

• Lead and implement projects eliminating waste using standard Manufacturing Engineering process.
• Verify Time standards prepared within ME Team.
• Update and report key Industrial Engineering metrics for assigned area.
• Drive process mapping activities within the assigned area.
• Drive SAP and Manufacturing Execution System standardization configurations.
• Prepare quotes for proposed projects within the assigned area.
• Drive process activities for New Product Introduction.

Job description

JOB SUMMARY

Manufacturing Engineer III will be responsible for planning, designing, implementing, and managing; integrated, production and service delivery systems that assure performance, reliability, maintainability, schedule adherence and cost control within the production site. The Manufacturing Engineer III will adopt as its goals profitability, effectiveness, adaptability, responsiveness, quality, and the continuous improvement of products and services throughout their life cycles.

ESSENTIAL DUTIES AND RESPONSIBILITIES

• Project leader – lead and implement projects that will eliminate waste, through the standard Manufacturing Engineering process
  • This will include but is not limited to: Complex Process Simulation, Operations Research and Business Model Cost Analysis
• Verify Time standards prepared within ME Team
• Update and report key Industrial Engineering metrics for assigned customer or area
• Drive key process mapping activities within the assigned customer or area
• Drive the standardization SAP and Manufacturing Execution System configurations
• Prepare quotes for proposed projects within the assigned customer or area
• Drive process related activities for New Product Introduction.
• Coach, mentor, and train engineers within the Manufacturing Engineering team
• Support and/or maintain all lower level Manufacturing Engineering essential duties and responsibilities
• Insure the standardization of Jabil processes throughout the site in accordance with the global, regional and site direction
• Support the Lean organization by developing a solid process foundation and data integrity in order to support process improvement through the organization
• Comply and follow all procedures within the company security policy.
• May perform other duties and responsibilities as assigned

JOB QUALIFICATIONS

KNOWLEDGE REQUIREMENTS

• Key Requirements:
  • Understanding and application of broad range of industrial engineering tools (ie. Work measurement, simulation, process mapping, facilities and workstation design, operations research, etc.)
  • Understanding of Jabil’s global strategies and direction
  • Understanding of site’s facilities, capabilities and how they tie back to the Jabil strategies and direction
  • Strong financial and analytical ability
  • Proven record of accomplishment of successful change management accomplishments, implementing and management continuous improvements and cost reduction programs
  • Strong communication skills
• Proficiency in use of personal computers, Microsoft Office products, Microsoft Visio, Microsoft Project, and AutoCAD skills required
• Experience and knowledge in Medical ISO 13485 and FDA Inspection will be highly recommended