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4 дня назад

Staff Development Engineer (MedTech)

109 000 - 174 800$
Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
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
Staff Development Engineer (MedTech): Developing assembly processes and equipment for handheld medical devices, from concept through stable production, with an accent on automation, equipment characterization, and regulatory compliance. Focus on designing assembly requirements, debugging and qualifying production stations, investigating manufacturing technologies, and coaching engineering teams.

Location: Cincinnati, Ohio, United States of America; up to 25% domestic and international travel may be required.

Base pay: $109,000–$174,800 per year.

Company

Johnson & Johnson MedTech develops healthcare technologies, including handheld surgical devices such as staplers, clip appliers, trocars, and sealing devices.

What you will do

  • Collaborate with product development teams, equipment suppliers, and manufacturing plants to deliver production solutions from concept through stable production.
  • Create assembly equipment requirements and provide design-for-assembly recommendations.
  • Develop, debug, characterize, and qualify assembly stations, including Factory Acceptance Testing.
  • Document equipment development activities according to medical-device procedures.
  • Investigate automation and other manufacturing technologies to improve processes and reduce time to market.
  • Coach engineers and support technical mastery, collaboration, and problem solving.

Requirements

  • Bachelor’s degree or equivalent experience in engineering.
  • 7+ years of experience in a dynamic R&D environment focused on production line development.
  • Experience developing manual and semi-automated assembly processes for small, complex components.
  • Experience with equipment debugging, characterization, Factory Acceptance Testing, qualification, GR&R, and software validation.
  • Strong communication, teamwork, influencing, and problem-solving skills.
  • Ability to execute projects in compliance with GMP, ISO, MDD, and internal procedures.

Nice to have

  • Medical-device or other regulated-environment experience.
  • Six Sigma or process excellence knowledge.
  • Vision systems, controls development, or automated assembly equipment experience.

Culture & Benefits

  • Inclusive work environment focused on employee dignity, diversity, and equal opportunity.
  • Retirement pension and 401(k) savings plans.
  • Long-term incentive program.
  • Vacation, sick time, holidays, personal and family time, parental, bereavement, caregiver, volunteer, and military spouse leave.
  • Opportunity to contribute to new product development and grow professionally.

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