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3 дня назад

Senior Engineer, Development (Medical Devices)

110 000 - 130 000$
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
Senior Engineer, Development (Medical Devices): Leading medical device product and process development from concept through sustaining with an accent on design for manufacturing, validation, and regulatory compliance. Focus on solving complex engineering problems, developing prototypes and test methods, and guiding cross-functional projects in breast care diagnostics.

Location: On-site in Cincinnati, Ohio, United States; travel up to 30% domestically and internationally, including occasional 2–5 day overnight assignments.

Salary: $110,000–$130,000 annually, plus eligibility for bonus or incentive pay.

Company

hirify.global’s Mammotome operating company develops breast care and breast cancer diagnostic technologies for clinicians, surgeons, and patients.

What you will do

  • Lead medical device product and process development from concept through sustaining in collaboration with suppliers, manufacturing engineers, design engineers, and cross-functional teams.
  • Drive design for manufacturing and assembly activities to optimize product designs and production readiness.
  • Qualify components, manufacturing processes, and assembly systems through validation activities.
  • Investigate product and process issues, perform root cause analysis, develop prototypes and test methods, and maintain engineering documentation and design controls.
  • Support product lifecycle planning, project execution, technical mentoring, and continuous improvement initiatives.

Requirements

  • Bachelor’s degree in Mechanical Engineering, Biomedical Engineering, or a related technical discipline.
  • Progressive engineering experience in product development, manufacturing, or a related technical discipline; 8+ years of relevant experience and 4+ years supporting product development and manufacturing are preferred.
  • Experience developing products in regulated or highly technical industries and applying quality and regulatory requirements throughout the product lifecycle.
  • Experience solving moderately complex engineering problems and leading small projects.
  • Experience with process validation, geometric dimensioning and tolerancing, and root cause analysis.
  • Ability to work on-site in Cincinnati and travel up to 30% domestically and internationally.

Nice to have

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

Culture & Benefits

  • Work within hirify.global’s continuous improvement system and engineering organization.
  • Paid time off and medical, dental, and vision insurance.
  • 401(k) benefits for eligible employees.
  • Reasonable accommodation is evaluated where needed.

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