✨ The Role in One Sentence

CUREosity GmbH is looking for a Working Student in Quality Management & Regulatory Affairs to support their quality standards and regulatory requirements in Düsseldorf.

📋 What You'll Likely Do

• 25%: Support the maintenance of the Quality Management System (QMS) according to ISO 13485.

• 25%: Assist in the creation and maintenance of technical documentation according to the Medical Device Regulation (MDR).

• 25%: Help with risk management, including identification, analysis, and evaluation of risks.

🧑‍💻 Profiles Doing This Job

• High Priority: Enrolled in a Master's program in Life Sciences, Medicine, or a natural science field.

• High Priority: Very good German (C2 level) and good English skills.

• High Priority: Structured, detail-oriented, and interested in quality management and regulatory requirements.

📈 How This Role Will Look on Your CV

• Supported quality management systems and regulatory affairs in an innovative Med-Tech startup.