Process Improvement Specialist

1 week ago


Bothell, Washington, United States Katalyst Healthcares & Life Sciences Full time
Job Summary:

As a Process Engineer Consultant at Katalyst Healthcares & Life Sciences, you will play a crucial role in driving process excellence and improving manufacturing operations. Your expertise will be instrumental in analyzing design, process, and quality issues, providing design feedback, and executing production readiness builds. You will also be responsible for creating line layouts, developing manufacturing assembly processes, and validating processes/documents for release. Additionally, you will assist in leading continuous improvement through Lean methodologies and provide training and technical support to enhance the skills of other engineers, technicians, and operators.

Key Responsibilities:

• Conduct root cause analysis of design, process, and quality issues found on the production floor during prototype builds.
• Evaluate and provide design feedback for ease of manufacturing & assembly.
• Execute production readiness builds, including creating line layouts and developing manufacturing assembly processes.
• Validate processes/documents for release and ensure compliance with regulatory requirements.
• Assist in leading continuous improvement through Lean methodologies, including identifying areas for improvement and implementing process changes.
• Provide training and technical support to enhance the skills of other engineers, technicians, and operators.

Requirements:

• Bachelor's degree in Industrial, Manufacturing, or Mechanical Engineering.
• Strong interpersonal and communication skills, with the ability to work effectively with cross-functional teams.
• Methodical, effective troubleshooting/problem-solving skills, with the ability to analyze complex issues and develop solutions.
• Experience with SolidWorks CAD design and ability to interpret engineering drawings.
• Work experience in an industrial environment, preferably in a Lean production environment.
• Excellent organizational and time management skills, with the ability to prioritize tasks and meet deadlines.
• Experience with FDA-regulated medical device manufacturing, Lean Manufacturing principles, and Microsoft Office tools.

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