Назад
Company hidden
8 дней назад

Lead Engineering Technician (Medical Devices)

85 300$
Формат работы
onsite
Тип работы
fulltime
Грейд
lead
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
Lead Engineering Technician (Medical Devices): Leading laboratory testing, method development, product evaluations, and failure investigations for new product development and product lifecycle management with an accent on technical leadership, regulatory compliance, and data analysis. Focus on validating test methods, mentoring laboratory personnel, coordinating cross-functional testing, and driving Lean Manufacturing and continuous improvement initiatives.

Location: Southington, Connecticut, United States; onsite laboratory role.

Salary: $85,300 annually.

Company

hirify.global provides staffing and employment opportunities for technical and engineering professionals.

What you will do

  • Provide technical leadership, training, mentoring, and oversight to laboratory technicians.
  • Coordinate testing priorities, resource allocation, and task execution across multiple projects.
  • Plan, conduct, and oversee moderate- to high-complexity laboratory testing.
  • Develop, validate, and document laboratory test methods, protocols, and standard operating procedures.
  • Perform product evaluations, returned product analysis, failure investigations, and technical reporting.
  • Lead Lean Manufacturing, 6S, and continuous improvement initiatives while maintaining laboratory compliance.

Requirements

  • Bachelor’s degree in engineering or a related technical discipline with at least 5 years of relevant experience, or an associate degree/technical certificate with at least 10 years of progressively responsible engineering technician experience.
  • Strong knowledge of engineering principles, testing methodologies, laboratory procedures, and data analysis.
  • Experience in a regulated manufacturing, testing, or medical device environment.
  • Experience leading, coordinating, and mentoring technical staff across multiple projects.
  • Knowledge of quality systems, documentation practices, and FDA, GMP, and ISO regulatory requirements.
  • Strong analytical, problem-solving, and cross-functional communication skills.

Culture & Benefits

  • Temporary assignments lasting 13 weeks or longer may include medical, dental, vision, and 401(k) benefits.
  • Statutory sick pay is provided where required.
  • Reasonable workplace accommodations are available for individuals with disabilities.
  • Equal employment opportunity and protected-veteran policies apply.

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 →