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14 часов назад

Manufacturing Engineer II (Medical Devices)

Формат работы
onsite
Тип работы
fulltime
Грейд
middle
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
Manufacturing Engineer II (Medical Devices) (Process Validation/Manufacturing Engineering): Developing, qualifying, and improving manufacturing processes for medical device production in Singapore with an accent on process validation, statistical process control, and regulatory compliance. Focus on leading qualification activities, solving manufacturing and equipment issues through root cause analysis, and implementing automation, inspection, and machine vision technologies.

Location: Singapore, Singapore; onsite work arrangement

Company

hirify.global develops healthcare technologies and medical devices serving patients across more than 150 countries.

What you will do

  • Lead manufacturing process qualification, validation, and verification activities supporting production readiness and process sustainability.
  • Develop, implement, and optimize manufacturing processes to improve quality, throughput, cost efficiency, and operational performance.
  • Analyze process performance using Statistical Process Control, process capability studies, and data-driven problem-solving methods.
  • Investigate manufacturing, equipment, and process issues, perform root cause analysis, and drive corrective actions.
  • Collaborate with Quality, Operations, Supply Chain, Research & Development, Engineering, and external suppliers.
  • Support manufacturing technologies including inspection systems, automation solutions, and machine vision applications.

Requirements

  • Bachelor's degree with 2+ years of experience in manufacturing engineering, process qualification, process validation, or production support in a regulated industry; or a master's degree with 0+ years of experience.
  • Experience executing process validation, verification, qualification, or manufacturing process development activities.
  • Experience applying Statistical Process Control, process capability analysis, or statistical methods to manufacturing processes.
  • Experience working cross-functionally with Quality, Operations, Supply Chain, Engineering, or external suppliers.
  • Knowledge of quality systems and regulatory requirements applicable to manufacturing environments.
  • Ability to work onsite in Singapore to support manufacturing operations, equipment, and process activities.

Nice to have

  • Experience in medical device, pharmaceutical, biotechnology, or other highly regulated manufacturing.
  • Experience with machine vision, automated inspection, manufacturing automation, supplier qualification, equipment qualification, or process transfer.
  • Knowledge of Lean Manufacturing, Six Sigma, or structured problem-solving methodologies.
  • Experience driving process standardization, manufacturing efficiency, or cost reduction initiatives.

Culture & Benefits

  • Work within a healthcare technology organization focused on improving patient outcomes.
  • Collaborate with cross-functional teams across manufacturing, quality, operations, supply chain, research and development, and suppliers.
  • Competitive compensation and a flexible benefits package.
  • Eligibility for the hirify.global Incentive Plan short-term incentive.

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