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Associate DCI Engineer (Medical Technology)

Формат работы
onsite
Тип работы
fulltime
Грейд
junior
Английский
b2
Страна
Mexico
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Associate DCI Engineer (Medical Technology): Advancing medical product design changes from concept to high-volume production with an accent on mechanical design, root-cause analysis, testing, and manufacturing efficiency. Focus on designing CAD components and assemblies, building test systems, implementing data-driven countermeasures, and maintaining GMP documentation under ISO 13485 and FDA requirements.

Location: Tijuana, Baja California, Mexico; onsite

Company

hirify.global is a medical technology company developing clinically differentiated orthopedic solutions, products, services, and integrated technologies.

What you will do

  • Advance product design changes from concept through high-volume production with cross-functional teams.
  • Perform hands-on and data-driven root-cause and countermeasure analysis for mechanical and soft-goods issues.
  • Design and build test systems to identify factory issues and customer complaint root causes.
  • Design, verify, and implement mechanical product changes and create CAD designs, diagrams, and layouts.
  • Work with Manufacturing to create processes, tests, and procedures that improve machine reliability and manufacturing efficiency.
  • Collaborate with Marketing to enhance legacy product designs and improve customer experience; maintain GMP documentation and follow engineering SOPs.

Requirements

  • Bachelor of Science degree in Mechanical Engineering or Industrial Engineering.
  • At least 1 year of experience in product development.
  • Proficiency in 3D modeling.
  • Intermediate spoken English, preferably at an advanced level.

Nice to have

  • Experience with SolidWorks or AutoCAD.

Culture & Benefits

  • Work in a cross-functional medical technology and manufacturing environment.
  • Follow Good Manufacturing Practices and Standard Operating Procedures.
  • Operate within ISO 13485, FDA, and other applicable manufacturing regulations.
  • Equal employment opportunities are provided based on merit, experience, and work-related criteria.

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