lean manufacturingcadprocess developmentmanufacturing engineeringstatistical process controlnew product introductionmedical devicesprocess validation
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Чётко очерченная стартовая инженерная роль в известной компании медицинских технологий даёт опыт запуска новых продуктов и регулируемого производства, но работа только на месте и требование неограниченного разрешения на работу в США существенно сужают доступ.
Жёсткие ограничения
Понятные задачи
Опыт в медтехе
Старт без стажа
Мэтч & Сопровод
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Manufacturing Engineer I (Medical Devices): Developing and improving manufacturing processes, equipment, tooling, production layouts, and process controls for Cranial & Spine new product introduction and ongoing operations with an accent on process readiness, qualification, manufacturability, and regulatory compliance. Focus on translating design requirements into scalable manufacturing solutions, optimizing production flow, and resolving equipment and process deficiencies.
Location: Humacao, Puerto Rico, United States of America; the role is based onsite and requires less than 25% travel.
Company
hirify.global develops healthcare technologies designed to alleviate pain, restore health, and extend life, serving patients across more than 150 countries.
What you will do
Support Cranial & Spine new product introduction and ongoing manufacturing operations.
Develop manufacturing processes, procedures, production layouts, equipment configurations, tooling, and operating sequences.
Translate product and design requirements into manufacturable, scalable process solutions with engineering, quality, operations, and supply chain teams.
Evaluate machinery, equipment, tooling, inspection requirements, and production readiness; implement corrective actions.
Support process development, qualification, validation, process controls, and Statistical Process Control where applicable.
Prepare manufacturing documentation and incorporate inspection, testing, compliance, and regulatory requirements into production plans.
Requirements
Bachelor’s degree in Engineering and 0 years of relevant experience.
Ability to work onsite in Humacao, Puerto Rico.
Ability to travel less than 25%.
For bachelor’s degrees earned outside the United States, the degree must satisfy the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A).
Roles below Principal level require unrestricted U.S. work authorization at hiring and throughout employment; sponsorship is not available for this role.
Nice to have
Bachelor’s degree in Mechanical, Manufacturing, Industrial, Electrical, Biomedical, or Chemical Engineering.
Internship, co-op, academic project, or professional experience in manufacturing engineering, new product introduction, process development, equipment, or tooling.
Knowledge of Statistical Process Control, process capability, or statistical manufacturing methods.
Knowledge of Design for Manufacturing, Lean Manufacturing, or continuous improvement methodologies.
Experience with Computer-Aided Design, medical device manufacturing, or regulated manufacturing environments.
Exposure to process validation, transfer activities, or launch support in a new product introduction setting.
Culture & Benefits
Full-time employment with a competitive salary and flexible benefits package.
Benefits and resources support employees across career and life stages.
Eligible for the short-term hirify.global Incentive Plan.
Reasonable accommodations are available for qualified individuals with disabilities.
Hiring process
Applications must be submitted through official hirify.global channels.
Legitimate recruiting communications come from approved hirify.global platforms and official @hirify.global.com email addresses; hirify.global does not request payment or sensitive personal information during early hiring stages.
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