Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Работа связана с производством медицинских изделий, но годовой контракт и противоречивые требования к опыту оставляют вопросы о стабильности и ожидаемом уровне специалиста.
Контракт на год
?Неясный уровень опыта
Медицинские технологии
Мэтч & Сопровод
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Process Engineer (1 Year Contract) Fresh Graduate Welcome to Apply! (Medical Manufacturing): Improving manufacturing processes and managing product, process, and label changes for medical products with an accent on process validation, industrial automation, and manufacturing efficiency. Focus on commissioning and debugging machinery, conducting feasibility and validation studies, implementing Lean and conservation projects, and resolving process issues through corrective and preventive actions.
Location: Singapore
Company
hirify.global develops vital organ therapy products and services, with a focus on kidney care, dialysis solutions, digital solutions, and advanced medical services.
What you will do
Manage product and process change projects, coordinating requirements, technical specifications, feasibility, schedules, implementation, and validation with stakeholders.
Support product design changes affecting product performance and lead change control, specification change, and validation activities.
Improve manufacturing process capability, predictability, machine performance, productivity, and production costs using Lean tools such as OEE.
Implement energy and water conservation projects, conduct process investigations and validation studies, and ensure stable, safe, environmentally responsible production.
Support manufacturing and maintenance engineering, including machinery commissioning, debugging, preventive maintenance planning, and corrective and preventive actions for customer complaints.
Manage label changes by coordinating feasibility, artwork and drawing updates, samples, supply chain, procurement, regulatory affairs, marketing, and product transitions.
Requirements
Degree in Mechanical Engineering, Mechatronic Engineering, or an equivalent discipline.
Degree with a minimum of 3 years of experience, while fresh degree graduates are welcome to apply.
2–3 years of experience in engineering project management and coordination.
Good engineering background in industrial automation, electrical engineering, and controls engineering.
Experience commissioning, debugging, and validating new manufacturing machinery.
Familiarity with basic GMP and other relevant requirements for medical or pharmaceutical product manufacturing.
Responsibility for compliance with Environment, Health & Safety procedures and requirements.
Nice to have
Knowledge of Installation Qualification, Operational Qualification, and Performance Qualification (IQ/OQ/PQ).
Culture & Benefits
Full-time, one-year contract position.
Work focused on improving patients’ lives through vital organ therapies and dialysis innovation.
Reasonable accommodations are available for candidates with disabilities during the application and interview process.
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