Technical Writer
vor 2 Wochen
Aufgaben
**Zu den Aufgaben gehören u.a.**:
- Schreiben, Formatieren, Bearbeiten, Überprüfen und Korrekturlesen von verfahrenstechnischen und technischen Dokumenten, einschließlich genomische Laborprotokolle und -berichte, SOPs, Testpläne und kundenseitige Dokumentation, alle im IVD-Bereich
- Vorbereiten von Tabellen und Diagrammen zur Visualisierung von Studiendaten
- Entwicklung und Abstimmung von Workflow-Diagrammen für Entwicklungsprozesse, einschließlich Entwicklung, Verifizierung, Validierung, klinische Studien, Registrierung und Vermarktung komplexer diagnostischer Produkte
- Unterstützung bei der Planung, Terminierung und Nachverfolgung von Dokumentationsarbeiten zur Einhaltung von Produktfreigabeterminen und Kundenvorgaben
- Weiterleitung von Dokumenten zur Überprüfung, Genehmigung oder Überarbeitung in einem EDMS
- Zusammenarbeit mit allen Ebenen des Unternehmens bei der Erstellung, Aktualisierung und Freigabe von Dokumentation
Qualifikation
- Bachelor-Abschluss in einem technischen Bereich
- Drei Jahre Erfahrung als Technischer Redakteur in der Pharma
- oder Diagnostikbranche; Erfahrung im Schreiben für IVD-Produkte ist ein Plus
- Erfahrung in der Erstellung von Dokumentationen für Zielgruppen mit unterschiedlichem technischem Kenntnisstand
- Ausgezeichnete Schreib-, Redaktions
- und Kommunikationsfähigkeiten in Deutsch und Englisch
- Fähigkeit, wissenschaftliche Dokumentationen im Bereich PCR-basierter IVD-Produkte zu lesen
- Erfahrung in der Präsentation technischer Informationen in Form von Schulungen, Präsentationen oder Videokonferenzen
**Benefits**:
- Attraktive Vergütung einschließlich Aktienoptionen
- Flexible Arbeitszeiten
- Flache hierarchische Strukturen
- Die Möglichkeit, in einem innovativen und hoch motivierten Team mitzuarbeiten
- 30 Tage Urlaub pro Jahr
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