Process Engineer III

US-CA-Rancho Santa Margarita

Overview

As a Process Engineer III, you will use skills related to sustaining and improving production manufacturing processes as part of a cross-functional team.


 


Responsibilities



  • Develop and sustain manufacturing processes

  • Debug manufacturing processes and equipment via root cause analysis

  • Run, observe and expedite shop orders

  • Develop and review engineering documents such as process maps, process FMEA, Manufacturing / Quality Instructions, Test Methods, drawings, and Test Reports

  • Investigate materials, manufacturing processes and technologies

  • Research and qualify new suppliers and vendors

  • Review and evaluate non-conforming materials, address customer experience reports, perform root cause analysis, and propose corrective/preventative actions

  • Provide technical guidance to other team members and train as necessary on manufacturing documentation, prototype generation and data analysis

  • Identify project critical paths in order to define project priorities and manage resources

  • Develop contingency plans for alternative project paths as necessary

  • Collaborate with production to identify capabilities and capacity

  • Collaborate with engineering team for fixturing and tooling design, tolerancing, and design for manufacturing

Position Requirements

Requirements



  • 3-5 Years of relevant Engineering work experience.

  • Bachelor’s Degree in Mechanical, Biomedical, Industrial, or Manufacturing Engineering (or equivalent) 

  • Experience with manufacturing equipment and processes

  • Experience with computer-aided design (i.e. SolidWorks), spreadsheets, scheduling programs, and word processing

  • Experience with Technical Writing



  • Experience with Statistical Process Control (SPC)

  • Working knowledge of Geometric Dimensioning and Tolerancing (GD&T)



  • Knowledgeable about a variety of materials and mechanical designs

  • Ability to effectively manage projects and work in cross-functional teams

  • Excellent written and verbal communication skills and ability to effectively present information

  • Technical aptitude and be detail oriented 


 


Preferred Qualifications



  • Experience in the medical device industry

  • Understanding of manufacturing and quality standards, including FDA regulations and ISO quality systems

  • Experience with software such as Netweaver / Product Life-Cycle Management

  • Experience with Minitab or statistical analysis software

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