7 дней назад
Global Manufacturing Engineer (MedTech)
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
Global Manufacturing Engineer (MedTech): Leading global manufacturing initiatives, including process innovation, multi-site process standardization, manufacturing digitization, and production transfers across Cytiva operations with an accent on validation, regulatory compliance, and process quality. Focus on defining machine requirements, managing project risks, and implementing cost-effective manufacturing improvements across global sites.
Location: Medemblik, Netherlands; on-site role with up to 15% global travel
Company
Cytiva is a operating company providing life sciences, diagnostics, biotechnology, and bioprocessing solutions for biological research, vaccines, medicines, and cell and gene therapies.
What you will do
- Lead global manufacturing initiatives involving process innovation, new process introduction, multi-site standardization, digitization, and production transfers.
- Collaborate with strategic, technical, operational, RD&E, and local engineering teams to define and implement manufacturing requirements.
- Define machine requirements and work with internal and external machine builders on equipment solutions.
- Manage supply chain considerations, product life cycle management, project risks, and mitigation plans.
- Determine validation requirements, develop validation and verification plans, execute analyses, and confirm acceptance.
- Identify manufacturing issues and implement cost-effective solutions that improve product quality, productivity, and regulatory compliance.
Requirements
- Bachelor’s degree in mechanical engineering, electrical engineering, industrial engineering, or a related technical field.
- At least 5 years of progressive post-bachelor’s experience in a related occupation.
- At least 5 years of experience in production or engineering, preferably in a regulated, medical device, or related industry.
- At least 5 years of project planning and project management experience, including managing multiple projects to completion.
- At least 3 years of experience in innovation, development, testing, and qualification.
- Valid driver’s license with an acceptable driving record and ability to travel globally up to 15%.
Nice to have
- Equipment automation theory and design experience.
- Experience manufacturing single-use technologies, consumables, mixers, or bioreactor hardware.
- Experience with lean manufacturing, design for manufacturing, 5S, 3P, root cause analysis, Six Sigma, and statistical tools.
Culture & Benefits
- Work within ’s continuous improvement system and a culture focused on belonging and collaboration.
- Contribute to solutions supporting life sciences, diagnostics, biotechnology, and human health.
- Eligible for bonus or incentive pay.
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