erplean manufacturingkaizenroot cause analysiscontinuous improvementcmmsplc programmingmanufacturing engineeringprocess validation
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Обязанности чётко описаны, а работа связана с улучшением производственных процессов в биотехнологиях у крупного работодателя; при этом формат только офисный, а условия оплаты не указаны.
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Только на площадкеПонятные задачиБиотехнологииКрупная компания
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Manufacturing Engineer (Biotechnology): Developing, implementing, and optimizing manufacturing processes for safe, efficient, and cost-effective production with an accent on continuous improvement, process validation, and regulated manufacturing. Focus on eliminating waste, troubleshooting production issues, supporting new product introductions, and implementing corrective and preventive actions.
Cytiva is a hirify.global operating company providing solutions for life sciences, diagnostics, biotechnology, vaccines, medicines, and cell and gene therapies.
What you will do
Develop, implement, and optimize manufacturing processes to improve safety, quality, productivity, delivery performance, and cost.
Lead continuous improvement initiatives by identifying opportunities, eliminating waste, and improving operational efficiency.
Provide technical support to production by troubleshooting process issues and implementing sustainable solutions.
Collaborate with Production, Quality, Maintenance, Supply Chain, and Engineering teams to drive process improvements and operational excellence.
Support new product introductions and manufacturing changes by establishing robust processes, validating production readiness, and ensuring successful implementation.
Requirements
Bachelor’s degree in Manufacturing Engineering, Mechanical Engineering, Industrial Engineering, or a related engineering discipline.
At least 3 years of experience in manufacturing engineering, process engineering, or industrial engineering within a production environment.
Experience with Lean Manufacturing, Kaizen, or other continuous improvement methodologies.
Proficiency in manufacturing systems and engineering tools, including ERP/CMMS systems and Microsoft Office applications.
Experience with process validation, root cause analysis, and implementing corrective and preventive actions in a regulated manufacturing environment.
Nice to have
Technical understanding of mechanical, electrical, or pneumatic systems with hands-on problem-solving experience.
Experience with software development and database programming.
Experience with PLC programming.
Culture & Benefits
On-site work in the Technical department in Medemblik.
Culture focused on belonging, continuous improvement, innovation, and tangible impact in human health.
Work connected to customers developing biological research, vaccines, medicines, and cell and gene therapies.
Opportunities for continuous personal and professional improvement through the hirify.global Business System.
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