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2 дня назад

Intern, NPI & Test Engineering (Medical Devices)

Тип работы
fulltime
Грейд
trainee
Английский
b2
Страна
Malaysia
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
Intern, NPI & Test Engineering (Medical Devices): Supporting new product introduction and test engineering activities in a medical device manufacturing environment with an accent on pFMEA risk remediation, process documentation, and quality compliance. Focus on analyzing process risks, tracking mitigation actions, coordinating cross-functional teams, and maintaining build protocols and reports.

Location: Gelang Patah, Johor, Malaysia; open only to Malaysian students

Company

hirify.global develops the Omnipod insulin management system and related drug-delivery technologies for people with diabetes and pharmaceutical partners.

What you will do

  • Support new product introduction activities and pFMEA remediation across manufacturing lines.
  • Review process risks and track remediation actions, owners, evidence, and closure status.
  • Update work instructions, process flow diagrams, control plans, and other manufacturing documentation.
  • Prepare project status reports and summarize findings for management review.
  • Participate in continuous improvement initiatives focused on process risk reduction and product quality.
  • Coordinate with Manufacturing, Quality, Operations, Engineering, design, development, testing, and production teams on build requirements and integration.

Requirements

  • Must be a Malaysian student enrolled in a BS or MS engineering program, or in the final year of an engineering or similar course.
  • Knowledge of Microsoft Office, including Word, Excel, PowerPoint, and Outlook.
  • Familiarity with data analytics tools.
  • Ability to maintain accurate records, demonstrate attention to detail, and follow rigorous processes.
  • Ability to adapt to changing work plans and equipment issues without compromising safety or quality.

Nice to have

  • Strong interpersonal and communication skills.
  • Fluency in English, Malay, or Mandarin.

Culture & Benefits

  • Exposure to industrial development and the medical device environment.
  • Work within a cross-functional engineering and manufacturing organization.
  • Operate in a cGMP-compliant environment under FDA 21 CFR 820 and ISO 13485 requirements.
  • Contribute to technologies designed to simplify diabetes management and drug delivery.

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