Industrial Engineering 3

Intuitive • Santa Clara, CA

8h

About The Position

Primary Function of Position The Industrial Engineer 3 (or IE 2) will help on delivering significant improvements in cost, manufacturability, capacity, and serviceability for robotic surgical instruments and accessories. The Industrial Engineer is responsible for leading continuous improvement projects, maintaining the plant layout, time studies, balancing production lines and strives to maintain gross efficiency metrics accuracy. Maintaining standard time for all products ensuring there is enough space availability and capacity installed as well as provide HC quantity needed to meet build plan among other industrial engineering related activities.

Requirements

• BS degree in Industrial/ Mechanical/ Electrical/ Electronic Engineering or equivalent
• Minimum 1-3 years, manufacturing, or process engineering experience with Mid/high volume manufacturing
• Demonstrate Lean Manufacturing and Six Sigma Green Belt knowledge
• Demonstrate ability in root cause analysis and continuous improvement
• Schedule oriented and demonstrate results based on such schedules (Plans / Gantt charts)
• Possess strong communication skills to interact with suppliers and other departments within the company (product development, planning, purchasing, regulatory, quality, etc…)
• MS in an Experience in Just-In-Time, Demand Flow Technology, and Lean Manufacturing techniques, 5’s Production Time Standard
• Strong examples of IE work; capacity planning, time flow, resource planning, line balancing, & bottleneck analysis
• Prior responsibility for process, equipment, or product validation/verification
• Prior experience with automated equipment, complex mechanism manufacturing, or robotics
• Able to read and understand mechanical and electrical drawings.

Nice To Haves

• Be of high character and energy with regard for detail
• Excellent communication skills, both written and verbal. Able to communicate eloquently up, down, and sideways.
• Demonstrate leadership skills to coordinate and coach other employees in continuous improvement activities.
• Demonstrate to be a self-directed employee with a minimum of supervision.
• Prior experience working in an FDA/ISO regulated environment.
• Experienced in ISO 13485 or medical device manufacturing environment.

Responsibilities

• Maintaining labor efficiency metrics accurate and actionable for the Mexicali site
• Leading continuous improvement projects
• Coaching and providing training on continuous improvement tools and methodologies DMAIC, root cause analysis, SPC, other statistical techniques, etc
• Perform Time studies to determine standard time and line balancing. Keep production time standards updated
• Maintaining the plant layout to improve productivity and capacity.
• Productivity improvement activities
• Waste reduction activities
• Train, develop, and motivate production personnel to follow procedures, meet high quality standards, production schedules, and productivity requirements.
• Ensure there is enough capacity installed to meet build plan.
• Elaborate VSM of critical processes
• Lead initiatives focused on yield improvement; Update documents as needed to maintain compliance with the quality system.
• Update of manufacturing methods in Work instructions (MPI)
• Operating procedures (SOP's, DOP's, etc.) creation and update
• Support SIOP cycle and MS initiatives related to capacity.
• Maintain capacity data accurate and updated.
• Plan, supervise, drive improvement, and report production performance including output, yields, root cause failures, efficiencies, and trends
• Assist in setting and attaining quarterly and annual production goals.
• Learn and enforce company safety policies and practices
• Equipment, Fixtures and Tools reliability challenge and provide design improvements proposals.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level