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6 дней назад

Senior R&D Engineer I-II (Medical Devices)

89 000 - 130 000$
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 R&D Engineer I-II (Medical Devices): Developing and commercializing medical device products and technologies across the product lifecycle with an accent on materials, processes, testing, and regulatory compliance. Focus on designing experiments, conducting verification and validation, performing risk and root-cause analysis, and transferring technologies into manufacturing.

Location: Libertyville, Illinois, United States

Salary: $89,000–$130,000 yearly

Company

hirify.global is an employee-owned healthcare products company developing, manufacturing, and marketing ostomy care, continence care, and critical care products worldwide.

What you will do

  • Lead or support research and development projects from feasibility and concept through prototyping, testing, verification, validation, and manufacturing transfer.
  • Identify, evaluate, and develop materials, processes, and technologies for new and existing medical device products.
  • Plan and execute laboratory, experimental, and product testing; analyze data and document conclusions and recommendations.
  • Create and review design specifications, drawings, protocols, reports, technical justifications, and other controlled documentation.
  • Conduct risk assessments, design reviews, feasibility studies, and root-cause analysis.
  • Collaborate with R&D, Manufacturing, Quality, Regulatory, Marketing, Market Access, Commercial, and legal teams.

Requirements

  • Bachelor’s degree in engineering, science, or a related technical discipline.
  • 5–8 years of related experience, preferably in industrial R&D, engineering, medical devices, pharmaceuticals, or another regulated industry.
  • Experience with product development, testing, technical documentation, design controls, and quality system environments.
  • Knowledge of regulatory standards and requirements, including ISO 13485, FDA, and EU MDR.
  • Ability to independently manage technical work packages or project elements with minimal supervision.
  • Demonstrated analytical thinking, structured problem-solving, technical judgment, and cross-functional communication skills.

Nice to have

  • Master’s degree or PhD in engineering or a related scientific discipline.
  • Experience with medical device design, development, or manufacturing.
  • Experience supporting intellectual property, patentability, or freedom-to-operate activities.
  • Experience leading projects or mentoring early-career engineers or students.

Culture & Benefits

  • Medical, prescription, dental, vision, disability, life, accident, and wellness benefits.
  • Paid parental and caregiver leave, statutory leave programs, paid holidays, vacation, and sick days.
  • 401(k) retirement plan with auto-enrollment, Roth contributions, vesting, and eligible safe-harbor matching contributions.
  • Education assistance, adoption assistance, and voluntary benefit programs.
  • Employee-owned environment focused on customer needs, collaboration, innovation, and meaningful outcomes.

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