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10 часов назад

Manufacturing Engineer (MedTech)

Тип работы
fulltime
Грейд
junior
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
Manufacturing Engineer (MedTech): Developing and optimizing manufacturing processes for spinal implants from raw material through final cleaning and shipment with an accent on process documentation, design for manufacturability, and production efficiency. Focus on reducing cycle time and waste, improving tooling and changeovers, and solving quality and cost challenges in a regulated medical-device environment.

Location: West Carrollton, Ohio, United States

Company

hirify.global develops medical technologies and spinal solutions designed to improve surgical techniques and patient outcomes.

What you will do

  • Lead projects for existing production families and coordinate cross-functional manufacturing launches for new and legacy products.
  • Develop and optimize processes for manufacturing spinal implants from raw material through final cleaning and shipment.
  • Create manufacturing documentation, including process FMEAs, control plans, process flows, work instructions, and inspection plans.
  • Improve machine and equipment efficiency through cycle-time reduction, waste elimination, tooling improvements, and changeover reduction.
  • Analyze and troubleshoot products and processes to reduce costs, improve quality, and increase efficiency.
  • Design, test, source, and cost-justify tooling, machinery, and equipment while supporting design-for-manufacturability reviews.

Requirements

  • Bachelor’s degree in engineering or a related discipline with at least 2 years of relevant experience, or an advanced degree without experience or equivalent work experience.
  • Fluency in print reading and GD&T, statistical process control, Lean Manufacturing, Six Sigma, Siemens NX or SolidWorks, and gage or fixture design.
  • Experience implementing and analyzing production performance metrics and KPIs.
  • Ability to communicate technical information, influence stakeholders, build consensus, and collaborate across functions.
  • Experience working in an environment regulated under 21 CFR 820 and/or ISO 13485.
  • Ability to meet the role’s physical requirements, including lifting up to 25 pounds occasionally and performing standing, climbing, kneeling, crouching, or crawling activities.

Culture & Benefits

  • Work is guided by innovation, customer focus, teamwork, and a results-driven approach.
  • Commitment to improving patient care through advanced medical technology.
  • Emphasis on respectful collaboration, accountability, inclusion, and ethical business practices.
  • Employment practices support equal opportunity and consideration for applicants regardless of protected characteristics.

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