Назад
Company hidden
3 дня назад

Associate Manufacturing Engineer (MedTech)

Формат работы
onsite
Тип работы
fulltime
Грейд
junior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
/
TL;DR
Associate Manufacturing Engineer (MedTech): Improving medical device manufacturing products and processes through engineering project planning, equipment troubleshooting, and process optimization with an accent on manufacturing efficiency, quality, and regulatory compliance. Focus on solving complex production problems, reducing downtime and waste, integrating new processes, and improving equipment utilization and yields across multiple shifts.

Location: Anasco, Puerto Rico, United States of America; onsite

Company

Johnson & Johnson MedTech develops smarter, less invasive, and more personalized healthcare and vision treatments.

What you will do

  • Coordinate manufacturing engineering projects from planning through implementation and completion within schedule and budget.
  • Develop and execute technical activities for new and improved medical device products and manufacturing processes.
  • Monitor equipment, machines, tools, and process parameters to address nonconforming products, low yields, quality issues, and equipment failures.
  • Optimize process output, throughput, equipment utilization, downtime, waste, yields, standard costs, and capital investments.
  • Provide technical troubleshooting support to manufacturing and collaborate with Quality, Research and Development, production, and customers.
  • Prepare project status reports, translate manufacturing data for leadership, and support training for new engineers and employees.

Requirements

  • Bachelor’s degree in Engineering.
  • 0–2 years of engineering experience preferred.
  • Fluent English and Spanish required.
  • Computer literacy required; knowledge of statistics and problem-solving or root-cause analysis preferred.
  • Understanding of FDA, ISO, OSHA, and other local and federal regulatory requirements preferred.
  • Availability for overtime, first-, second-, and third-shift schedules, including weekends and holidays, required.

Nice to have

  • Experience in the medical device or pharmaceutical industry.
  • Basic knowledge or certification in Lean and Six Sigma methodologies.

Culture & Benefits

  • Inclusive work environment focused on respect, dignity, diversity, and individual contribution.
  • Work is performed onsite with varied production schedules and shift coverage.
  • Equal opportunity employment and an interview process with accommodation support for applicants with disabilities.

Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →