Technical Documentation Intern
Job Summary
Job Description
The Technical Documentation Intern will process customer complaints, conduct data mining, and generate reports for design enhancement insights. They will prepare material attribute data for sustainability tasks and assist R&D engineers with CAPA tasks and maintaining documentation for medical devices, including translation. The intern will also compare and report on the differences between China Medical Device regulations (NMPA) and other regulations (FDA, EUMDR, etc.). This role requires excellent English skills, a background in engineering or related fields, and the ability to work 3-5 days a week for a 2-month internship.
Must have:
- Excellent English skills in listening, speaking, reading, and writing.
- Currently pursuing a Bachelor's degree or higher.
- Self-motivation, self-management, and execution ability.
- Fluent in Microsoft Office tools (Word, Excel, PowerPoint).
Good to have:
- Engineering education background is a plus.
- Healthcare and/or Medical Science background would be a plus.
3 skills required
Job Details
Job Title
Technical Documentation InternJob Description
Your role:
• Process customer complaints, conduct data mining and report generation for meaningful design enhancement insights.
• Prepare material attribute data for sustainability tasks (Extended producer responsibility).
• Assist R&D engineer for ongoing CAPA tasks.
• Assist R&D engineer in maintaining documentation for medical devices. Translate related documents, ensure translation integrity and consistency.
• Read, compare and list the content difference between China Medical Device regulation (NMPA) and others (FDA, EUMDR, etc.), and form reports for team review.
• Other tasks assigned by team & company.
• Process customer complaints, conduct data mining and report generation for meaningful design enhancement insights.
• Prepare material attribute data for sustainability tasks (Extended producer responsibility).
• Assist R&D engineer for ongoing CAPA tasks.
• Assist R&D engineer in maintaining documentation for medical devices. Translate related documents, ensure translation integrity and consistency.
• Read, compare and list the content difference between China Medical Device regulation (NMPA) and others (FDA, EUMDR, etc.), and form reports for team review.
• Other tasks assigned by team & company.
You're the right fit if:
• Currently pursuing a Bachelor's degree or higher.
• Excellent English skill in listening, speaking, reading and writing.
• Engineering education background, Healthcare and/or Medical Science background would be a plus.
• Available to work 3-5 days per week, with an internship duration of 2 months.
• Self-motivation, self-management and sound ability of execution.
• Fluent in Microsoft Office tools (Word, Excel, PowerPoint, etc.)
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About The Company
At Philips, we believe that every human matters. As a global health-tech leader, we focus on improving people’s health and wellbeing through meaningful innovation. The people who work here share our passion and are motivated to bring this purpose to life.For more than 130 years, we have been creating technologies and innovations that improve people's lives and support healthcare practitioners. Headquartered in the Netherlands and operating in more than 100 countries globally, we focus our advanced technology and deep clinical and consumer insights on Precision Diagnosis, Image Guided Therapy, Enterprise Informatics, Monitoring/ Connected Care, Sleep & Respiratory Care and Personal Health.Together, we deliver better care for more people because we believe that every human matters.
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