Regulatory Affairs Specialist

EPM Scientific; München; Hybrid; EUR 60.000 - 80.000; Vollzeit

Zusammenfassung

A leading Medical Device Company in Bavaria is seeking a Regulatory Affairs Specialist for a hybrid role. The successful candidate will support regulatory submissions and compliance activities, ensuring alignment with EU and international medical device regulations. Candidates should have proven experience in regulatory affairs in medical equipment manufacturing. This position is for a 12-month contract with a start date as soon as possible.

Qualifikationen

• Proven experience in regulatory affairs within medical equipment manufacturing companies.

Aufgaben

• Support regulatory submissions and compliance activities.
• Ensure alignment with EU and international medical device regulations.

Kenntnisse

Regulatory Affairs experience in medical equipment

Jobbeschreibung

Regulatory Affairs Specialist - Medical Device Manufacturing Project (Bavaria 🇩🇪)

We're hiring Regulatory Affairs Specialists for a major medical device manufacturing project based in Bavaria! Join a leading Medical Device Company in a hybrid role supporting regulatory submissions, compliance activities, and alignment with EU and international medical device regulations.

📍 Location: Bavaria (hybrid)

📅 Duration: 12-month contract

🚀 Start: ASAP

🔍 Key Requirements

• Proven experience in regulatory affairs within medical equipment manufacturing companies