Regulatory Affairs Specialist – Medical Devices, Switzerland

Teleflex Incorporated; Bülach; Vor Ort; CHF 75’000 - 95’000; Vollzeit

Zusammenfassung

A global provider of medical technologies seeks a dedicated team member for regulatory affairs to assist in product registration and maintain documentation for innovative vascular intervention devices. This role requires a university degree in a relevant field, teamwork, analytical skills, and fluency in English, with proficiency in German being a plus. Knowledge of Microsoft Office and SAP is preferred. Join a company focused on improving healthcare through diversity and inclusion.

Qualifikationen

• One year of experience with registrations of medical devices is a plus.
• Fluency in English is mandatory; German and any additional language are an advantage.

Aufgaben

• Supporting product registrations in low-effort countries.
• Maintaining the project status of registrations in the regulatory database.
• Assessing and clarifying requirements for new device registrations.

Kenntnisse

Microsoft Office

Adobe applications

Analytical skills

Teamwork

Attention to detail

Ausbildung

University degree in natural sciences, pharmacy, pharmacology, medicine or engineering

Tools

SAP

Jobbeschreibung

A global provider of medical technologies seeks a dedicated team member for regulatory affairs to assist in product registration and maintain documentation for innovative vascular intervention devices. This role requires a university degree in a relevant field, teamwork, analytical skills, and fluency in English, with proficiency in German being a plus. Knowledge of Microsoft Office and SAP is preferred. Join a company focused on improving healthcare through diversity and inclusion.