manufacturinggmpmaintenancevalidationequipment engineeringequipment qualificationroot cause analysisreliability engineeringchange controlfmea
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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В Company hidden чётко очерчена роль инженера по оборудованию в регулируемом производстве медтехники: обязанности конкретны, а компания и рабочая среда понятны.
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Понятные задачиПольза для медициныКрупный работодатель
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Мэтч & Сопровод
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Equipment Engineer (Medtech): Supporting equipment life cycle management, maintenance programs, and reliability improvement for medical device manufacturing with an accent on qualification, validation, compliance, and equipment performance. Focus on coordinating equipment acquisition and retrofit projects, applying root cause analysis, and implementing corrective and preventive actions for equipment failures and deviations.
Location: Onsite in Lausanne, Vaud, Switzerland
Salary: CHF 82,320–123,480 per year
Company
Global healthcare technology organization developing and manufacturing medical devices.
What you will do
Support projects improving equipment reliability, efficiency, compliance, performance, and sustainability.
Coordinate with equipment vendors and suppliers on procurement, installation, characterization, qualification, and validation.
Contribute to equipment replacement and retrofit initiatives.
Develop and enhance preventive and predictive maintenance strategies with maintenance teams.
Collaborate with manufacturing, quality, maintenance, and regulatory teams on project execution, change control, and compliance.
Investigate equipment failures and deviations, apply root cause analysis tools, and support CAPA implementation while providing technical support and training.
Requirements
Bachelor’s degree in Engineering, such as Mechanical, Electrical, Manufacturing, or a related field.
Several years of equipment engineering experience in a manufacturing environment.
Experience with equipment life cycle management, maintenance programs, and reliability improvement.
Experience supporting equipment improvement, replacement, qualification, or validation projects.
Good understanding of equipment qualification and validation processes.
Familiarity with change control procedures and manufacturing regulatory requirements, including FDA, ISO, and GMP standards.
Project coordination experience with the ability to manage priorities and deliverables.
Strong analytical, problem-solving, and technical troubleshooting skills related to equipment performance and reliability.
Effective communication and collaboration skills, including the ability to build productive relationships with vendors, suppliers, and internal stakeholders.
Culture & Benefits
Onsite work in an innovative industrial medical-device manufacturing environment.
Competitive salary and flexible benefits package.
Benefits and resources designed to support employees across career and life stages.
Work focused on healthcare technology, patient impact, growth, and continuous improvement.
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