QA/RA Intern - QMS Migration for Healthcare Software

FarMedvisie B.V.

Woerden

Remote

EUR 5,100 - 6,100

Part time

3 days ago
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Benefits offered by this job

Internship allowance
Confluence exposure
Small team environment
Future opportunities
ISO 13485 training

Job summary

FarMedvisie B.V. in Woerden, Netherlands, is seeking a QA/RA Intern to support a major QMS improvement project and Confluence migration.

You will help structure procedures, ensure documentation accuracy, and maintain version control under supervision, while gaining hands-on experience in ISO 13485 and MDR compliance. We welcome HBO and WO students from related fields who are fluent in Dutch and English, detail-oriented, and able to commit to at least three days per week.

Qualifications

  • HBO or WO student in a related field.
  • Fluent in Dutch and English, written and spoken.
  • Excellent attention to detail and strong organizational skills.
  • Able to work independently and maintain focus on detailed tasks.
  • Willing to learn Confluence and document management.
  • Comfortable using Microsoft Office and digital documentation tools.

Responsibilities

  • Update, structure and standardize procedures and quality documents.
  • Check documentation for accuracy, completeness and consistency.
  • Support document control, version management and traceability.
  • Apply predefined templates and documentation standards.
  • Monitor migration progress and maintain task overviews.
  • Identify missing or inconsistent information and flag it for review.
  • Support the Quality & Regulatory team with related improvement activities.

Skills

Dutch language
English language
Attention to detail
Organizational skills
Independent work

Education

HBO/WO student in related field

Tools

Confluence
Microsoft Office

Job description

FarMedvisie B.V. in Woerden, Netherlands, is seeking a QA/RA Intern to support a major QMS improvement project and Confluence migration.

You will help structure procedures, ensure documentation accuracy, and maintain version control under supervision, while gaining hands-on experience in ISO 13485 and MDR compliance. We welcome HBO and WO students from related fields who are fluent in Dutch and English, detail-oriented, and able to commit to at least three days per week.

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