2 дня назад
Intern, NPI & Test Engineering (Medical Devices)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
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
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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