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Process Engineer (1 Year Contract) (Medtech Manufacturing)

Формат работы
onsite
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
Singapore
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
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TL;DR
Process Engineer (Medtech Manufacturing): Managing product and process changes while improving manufacturing capability, machinery performance, and production costs with an accent on Lean tools, industrial automation, validation, and medical-product requirements. Focus on commissioning and debugging manufacturing machinery, conducting process investigations, implementing corrective actions, and coordinating label changes across regional operations.

Location: Singapore

Company

hirify.global develops vital organ therapy solutions, including digital and advanced services that support kidney care and dialysis.

What you will do

  • Manage product and process change projects, coordinating requirements, technical specifications, schedules, feasibility, implementation, and validation with stakeholders.
  • Lead change control, specification change, product design change, and validation activities.
  • Improve manufacturing process capability, predictability, machine performance, and production costs using Lean tools such as OEE.
  • Conduct feasibility studies, process investigations, machinery validation, and projects focused on energy and water conservation.
  • Support manufacturing and maintenance engineering, including machinery commissioning, debugging, parts-life analysis, and preventive maintenance planning.
  • Coordinate label changes with plant operations, quality, planning, supply chain, marketing, procurement, vendors, and regulatory affairs.

Requirements

  • Degree in Mechanical Engineering, Mechatronic Engineering, or an equivalent discipline.
  • At least 3 years of relevant engineering experience, including 2–3 years in engineering project management and coordination.
  • Strong engineering background in industrial automation, electrical engineering, and controls engineering.
  • Experience commissioning, debugging, and validating new manufacturing machinery.
  • Familiarity with basic GMP and other requirements for medical or pharmaceutical product manufacturing.
  • Compliance with EHS 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 patient and care-team outcomes in vital organ therapy.
  • Commitment to providing reasonable accommodations for candidates with disabilities.

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