Senior DFM Process Engineer - Medical Device Innovation

Align Technology, Inc.

Ciudad Juárez

On-site

MXN 900,000 - 1,300,000

Full time

9 days ago

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Job summary

Align Technology, Inc. is seeking a Senior DFM Process Engineer to lead design for manufacturing improvements at the Juarez plant. You will work with R&D, product design, and manufacturing teams to optimize processes, validate changes, and ensure quality and compliance in a regulated medical device environment.

The role emphasizes root-cause analysis, design of scalable processes, and collaboration across global teams to meet business goals.

Qualifications

  • Bachelor-level engineering degree in one of the listed fields.
  • Minimum of 5 years of experience in a similar position.
  • Six Sigma certifications: Master Black Belt, Black Belt, or Green Belt.
  • Experience in medical/pharmaceutical industry regulated by the FDA.
  • Experience in Manufacturing Process Design and New Product Introduction.

Responsibilities

  • Leads and supports global teams across R&D, design, and manufacturing.
  • Conducts root cause analysis of process issues and tests changes.
  • Designs experiments to evaluate production change feasibility.
  • Establishes operational ranges and control limits for process stability.
  • Communicates progress and provides guidance on engineering changes.
  • Supports investigations of field customer complaints and risk assessments.

Skills

Attention to detail
Critical thinking
English proficiency
AGILE/SCRUM

Education

Mechatronics Engineering
Mechanical Engineering
Electrical Engineering
Electronic Engineering
Computer Science Engineering
Industrial Engineering
Science Engineering

Tools

ANSYS
Abaqus
COMSOL
MATLAB
SolidWorks
MS Office Suite

Job description

Align Technology, Inc. is seeking a Senior DFM Process Engineer to lead design for manufacturing improvements at the Juarez plant. You will work with R&D, product design, and manufacturing teams to optimize processes, validate changes, and ensure quality and compliance in a regulated medical device environment.

The role emphasizes root-cause analysis, design of scalable processes, and collaboration across global teams to meet business goals.

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