INTERNSHIP DETAILS
Werkstudent Forschung & Entwicklung - Technische Dokumentation (m/w/d)
Companyaap Implantate AG
LocationBerlin
Work ModeOn Site
PostedFebruary 23, 2026

Internship Information
Core Responsibilities
The role involves assisting in the creation of technical documentation for medical devices of Class I-IIb, as well as helping to structure and standardize documents. Responsibilities also include conducting, evaluating, and documenting various tests and supporting the further development of existing products.
Internship Type
part time
Company Size
52
Visa Sponsorship
No
Language
German
Working Hours
40 hours
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About The Company
aap Implantate AG is a globally operating medical device company headquartered in Berlin, Germany. The company develops, manufactures and markets trauma products for orthopedics. The IP protected portfolio includes besides the innovative anatomical plating system LOQTEQ® and trauma complementary biomaterials a wide range of cannulated screws as well as standard plates and screws. Furthermore, aap Implantate AG has an innovation pipeline with promising development projects as the antibacterial silver coating technology and magnesium based implants. These technologies address critical problems in surgery that haven’t yet been resolved adequately. In German-speaking Europe aap Implantate AG directly sells its products to hospitals, buying syndicates and hospital groups while it has a broad network of distributors in more than 20 countries at the international level.
aap Implantate AG is a stock listed company. Its share is quoted in the General Standard segment of Frankfurt Stock Exchange (XETRA: AAQ.DE).
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About the Role
Ihre Aufgaben
- Mitarbeit bei der Erstellung der technischen Dokumentation für Medizinprodukte der Klasse I-IIb
- Mitarbeit bei der Strukturierung und Standardisierung von Dokumenten
- Durchführung, Auswertung und Dokumentation verschiedener Tests
- Unterstützung bei der Weiterentwicklung bestehender Produkte
Ihr Profil
- Eingeschriebener Student (m/w/d) im Bereich Medizintechnik, Naturwissenschaften oder einem vergleichbaren (Ingenieurs-)studiengang
- langfriste Anstellung gewünscht, mindestens 12 Monate
- Technisches Verständnis und strukturierte Arbeitsweise
- Kenntnisse über regulatorische Anforderungen (MDR (EU 2017/745)) von Vorteil
- Hohe Sorgfalt im Umgang mit Daten und Dokumenten
- Sehr gute Deutsch- und Englischkenntnisse in Wort und Schrift
- Sicherer Umgang mit MS Office Anwendungen (Word/Excel)
Warum wir?
Wir bieten:
- Eine abwechslungsreiche Arbeit in einer zukunftsweisenden Branche
- Flexible Arbeitszeiten
- Eine leistungsgerechte Entlohnung
- Ein hoch motiviertes Team
- Sehr gute Anbindung an die öffentlichen Verkehrsmittel
Key Skills
Technical DocumentationMedical DevicesStructuringStandardizationTestingProduct DevelopmentRegulatory RequirementsMDR (EU 2017/745)Data HandlingMS OfficeWordExcel
Categories
HealthcareScience & ResearchEngineering
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