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20 часов назад

Sr/Process Engineer (Medical Manufacturing)

Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
Singapore
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Sr/Process Engineer (Medical Manufacturing): Managing product and process change projects and improving manufacturing processes with an accent on industrial automation, Lean tools, equipment validation, and regulatory compliance. Focus on commissioning and debugging manufacturing machinery, conducting IQ/OQ/PQ validation studies, implementing corrective actions, and reducing production costs while maintaining safety and product quality.

Location: Singapore

Company

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

What you will do

  • Manage product and process change projects, coordinating requirements, technical specifications, feasibility, schedules, implementation, and validation with stakeholders.
  • Lead change control, specification changes, product design changes, and validation activities.
  • Improve manufacturing process capability, machine performance, productivity, predictability, and production costs using Lean tools such as OEE.
  • Implement energy and water conservation initiatives and maintain stable, safe, environmentally responsible processes that meet product requirements.
  • Support manufacturing and maintenance engineering, including machinery commissioning, debugging, process investigations, corrective and preventive actions, and technician coordination.
  • Coordinate label changes with plants, quality, planning, supply chain, marketing, procurement, vendors, and regulatory affairs, including label artwork and product sample verification.

Requirements

  • Degree in Mechanical or Mechatronic Engineering, or an equivalent qualification.
  • At least 3 years of relevant experience, including 2–3 years in engineering project management and coordination.
  • Strong 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 manufacturing.
  • Responsible for compliance with EHS procedures and requirements.

Nice to have

  • Knowledge of Installation Qualification, Operational Qualification, and Performance Qualification (IQ/OQ/PQ).

Culture & Benefits

  • One-year full-time contract.
  • Work focused on improving patients’ lives through vital organ therapies.
  • Reasonable accommodations are available for candidates with disabilities during the application and interview process.

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