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3 дня назад

Staff Engineer, Development (Medical Devices)

135 000 - 160 000$
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 Engineer, Development (Medical Devices): Leading complex medical device development and manufacturing initiatives from concept through sustaining with an accent on design for manufacturing, component qualification, validation, and regulatory compliance. Focus on solving advanced technical challenges, improving products and processes, and providing technical leadership across cross-functional engineering teams.

Location: On-site in Cincinnati, Ohio, United States. Travel of up to 30% domestically and internationally may be required, including overnight stays of 2 to 5 days.

Salary: $135,000–$160,000 annually, plus bonus or incentive pay.

Company

hirify.global operates Mammotome, a medical technology business focused on breast care, diagnostics, and products that support improved patient outcomes.

What you will do

  • Lead complex medical device development and strategic engineering initiatives from concept through sustaining.
  • Collaborate with suppliers, manufacturing engineers, design engineers, and cross-functional stakeholders.
  • Lead design-for-manufacturing and assembly analyses and integrate findings into product concepts.
  • Qualify complex components, manufacturing processes, and assembly systems through appropriate validation methodologies.
  • Drive product and process improvements, engineering standards, structured problem solving, and risk mitigation.
  • Influence product strategy and technology roadmaps while providing technical leadership and mentorship.

Requirements

  • Bachelor’s degree in Mechanical Engineering, Biomedical Engineering, or another technical discipline.
  • Progressive engineering experience in product development, manufacturing, or related technical disciplines; 10 or more years of relevant experience is preferred, including 6 or more years in product development and manufacturing.
  • Experience developing products in regulated or highly technical industries and applying quality and regulatory requirements throughout the product lifecycle.
  • Experience leading technical initiatives, engineering projects, or cross-functional teams and solving complex technical challenges.
  • Experience with design, development, validation, product lifecycle activities, structured problem solving, and engineering project management in regulated environments.
  • Ability to work on-site in Cincinnati, Ohio, United States.

Nice to have

  • Medical device development experience, including design for manufacturability and regulatory compliance.
  • Master’s degree in engineering or a related field.
  • Advanced Six Sigma or Project Management Professional certification.

Culture & Benefits

  • Paid time off and comprehensive medical, dental, and vision insurance.
  • 401(k) plan for eligible employees.
  • Bonus or incentive pay eligibility.
  • Work within a cross-functional engineering team focused on breast care, diagnostics, and patient outcomes.
  • Reasonable accommodations are evaluated where needed.

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