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Manufacturing Engineer I

Haemonetics

Tijuana

Presencial

MXN 400,000 - 600,000

Jornada completa

Hace 2 días
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Descripción de la vacante

A leading healthcare solutions company based in Tijuana, Mexico is seeking a professional responsible for developing and implementing product design enhancements and manufacturing process improvements. The ideal candidate will manage documentation and handle time studies to boost efficiency. A dynamic work environment encourages innovative approaches to solving manufacturing challenges. Join a diverse team committed to quality and efficiency in healthcare solutions.

Formación

  • Experience in developing product design changes.
  • Ability to implement manufacturing process improvements.
  • Proficiency in generating necessary documentation.

Responsabilidades

  • Develop and implement changes to product design.
  • Conduct time studies and revise line layouts.
  • Generate required documentation for Engineering Change Orders.

Conocimientos

Process improvement
Documentation management
Data analysis
Automation implementation
Descripción del empleo

We are constantly looking to add to our core talent. If you are seeking a career that is challenging and rewarding, a work environment that is diverse and dynamic, look no further — Haemonetics is your employer of choice.

Job Details

Responsible to develop and implement changes to product design and/or to the manufacturing process to achieve significant quality, efficiency or cost improvements. This requires participation in new product development programs, identifying design-for-manufacturability issues and ensuring these issues are addressed prior to release, including:

  • Complete time studies, revise line layouts, and implement selective automation to improve efficiency
  • Develop and gain approvals for all test protocols
  • Develop corrective actions to resolve issues and implement changes
  • Follow up to ensure problem is resolved
  • Generate all the required documentation (Drawings and BOM’s, Manufacturing Instructions, 510K review, Costing, Implementation Analysis) required to submit an Engineering Change Order
  • Implement changes and complete operator training
  • Implement changes to Manufacturing upon ECO approval
  • May lead small scope projects under the direction and supervision of manager
  • Perform or facilitate all the required testing as specified in the protocol
  • Responsible for documentation and implementation of approved changes
  • Review and analyze and document test results in a test report
  • Review and chart customer and in process defect data and identify highest frequency and most critical failure modes
  • Review assembly processes for opportunities to improve efficiency and throughput
  • Other duties as assigned

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