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11 дней назад

Manufacturing Engineer I (Shift A M-S 6 am a 2 pm) (Medtech)

Формат работы
onsite
Тип работы
fulltime
Грейд
junior
Английский
b2
Страна
CR
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Мэтч & Сопровод

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Описание вакансии

Текст:
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TL;DR
Manufacturing Engineer I (Medtech): Developing robust manufacturing solutions and improving medical device production processes in cleanroom environments with an accent on product quality, equipment performance, GMP, and ISO 13485 compliance. Focus on hands-on process engineering, resolving production floor issues, and implementing continuous improvements with cross-functional teams.

Location: On-site in Cartago, Costa Rica. Shift A runs Monday through Saturday from 6:00 am to 2:00 pm.

Salary: ₡0–₡0 per month

Company

hirify.global develops medical device products and manufacturing solutions.

What you will do

  • Provide manufacturing technology and robust solutions to commercialize new products.
  • Perform hands-on process engineering in cleanroom environments.
  • Collaborate with cross-functional teams to resolve production floor issues.
  • Optimize product quality, equipment performance, and manufacturing processes.
  • Implement continuous improvement initiatives in compliance with GMP and ISO 13485 standards.

Requirements

  • Bachelor’s degree in Mechanical, Biomedical, Electrical, Chemical, Materials, or Industrial Engineering.
  • At least one year of engineering experience.
  • English proficiency at B2 level is required for regular interaction with global teams and English documentation.
  • Excellent written, verbal, and interpersonal communication skills.
  • Competence with CAD software and Microsoft Office, including Excel, PowerPoint, and Word.

Nice to have

  • Experience in a manufacturing environment, preferably in the medical device industry.
  • Knowledge of FDA regulations, Lean or Flow Manufacturing, materials, and manufacturing processes.

Culture & Benefits

  • On-site engineering work in a cleanroom manufacturing environment.
  • Regular collaboration with global teams and cross-functional production groups.
  • Focus on product quality, equipment performance, regulatory compliance, and continuous improvement.

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