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Manufacturing Engineer

Orange County Metro Area, CA

Post Date: 11/09/2017 Job ID: JN -112017-20398 Job Type: Scientific
The Process Engineering role will primarily be responsible for re-formatting / simplifying process instructions, procedures, and documentation of existing products to conform to a yet to be identified best-practice standard. Additional responsibilities include but are not limited to:
  • Work cross functionally to strategically define best-practice standard
  • Perform time studies, data collection, and process analysis to understand & capture current state
  • Analyze operations and sequence of operations to identify non-value added steps & eliminate waste
  • Re-format / simply existing process documentation to improve clarity, conciseness, and accuracy per best-practice standards
  • Tailor instructions for 1st generation ESL target audience group
  • Perform requalification activities as necessary (Process Verification, Validation, etc )
  • Collaborate with product lines to seamlessly implement changes with no business disruptions
  • Experience / interest in a Lean/Continuous Improvement focused role
  • Excellent communication skills and ability to work independently with strong leadership
  • Ability to analyze and solve problems by thinking strategically and creatively
  • Additional strengths include strong initiative, critical thinking skills and understanding of medical device manufacturing and compliance.
  • Risk management as it applies to logistics and timeline
  • Excellent interpersonal skills with team members, management, and executive staff.
  • Ability and comfort working in matrix resources.
  • Excellent influence and change management skills.
  • Medical device experience is a plus
Bachelor of Science degree in Engineering (Mechanical or Industrial preferred) or scientific field

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