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4 дня назад

Manufacturing Engineer III (Medical Devices)

109 000 - 152 000$
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
Manufacturing Engineer III (Medical Devices): Developing, validating, and improving manufacturing processes and electromechanical products in a medical device production environment with an accent on supplier coordination, quality systems, and process optimization. Focus on root cause analysis, PCBA qualification testing, process validation, and implementing solutions that improve yield, efficiency, and throughput.

Location: Alameda, California, United States; on-site

Annual base salary: $109,000–$152,000

Company

hirify.global develops medical devices and operates manufacturing engineering programs focused on commercializing new products and improving production.

What you will do

  • Design, execute, and document test plans for PCBA components, processes, equipment, raw materials, and products.
  • Perform root cause analysis and troubleshoot electromechanical products, recommending and implementing effective solutions.
  • Develop, characterize, validate, and optimize manufacturing processes using statistical techniques and engineering knowledge.
  • Manage NCRs, deviations, engineering change orders, supplier documentation, and quality system records.
  • Lead supplier-level projects, coordinate communications and timelines, and ensure project milestones are met.
  • Support production through process documentation, equipment monitoring, training, and continuous improvement initiatives.

Requirements

  • Bachelor’s degree in Electrical, Biomedical, Mechanical, Chemical, Materials, Industrial Engineering, or a related field, plus 4+ years of relevant engineering experience, or an equivalent combination of education and experience.
  • Experience in a manufacturing environment; medical device industry experience is preferred.
  • Knowledge of FDA regulations, Lean or flow manufacturing, and materials and manufacturing processes is desirable.
  • Strong written, verbal, interpersonal, and cross-functional communication skills.
  • Proficiency with Word, Excel, PowerPoint, Access, and other computer applications.
  • Ability and willingness to work on site in Alameda, California.

Culture & Benefits

  • Work across production, engineering, quality, suppliers, and other functional groups.
  • Work in office, laboratory, and clean room environments.
  • Benefits and equity program may be available in addition to base compensation.
  • Business travel is expected at 0%–10%.
  • Role includes occasional lifting and moving of items up to 25 pounds and movement between buildings and floors.

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