Ihr Team bei Metecon

Rechnen Sie mit den Besten

Auf dem weiten Feld der Regulatory Compliance sind wir zuhause: Technische Dokumentation und Qualitätsmanagement, Clinical Affairs und Regulatory Affairs, Medical Device Software sowie Verifikation und Validierung beherrscht unser über 50-köpfiges Team aus dem Effeff.

Ihre Expert*innen bei Metecon - allesamt Ingenieur*innen und Naturwissenschaftler*innen - verfügen über fundiertes klinisches und regulatorisches Know-how, Erfahrung in Mechanik, Elektronik und Software sowie über umfassende Projektmanagementfähigkeiten. Wir ebnen den Weg für Ihr Medizinprodukt oder IVD. Und Sie erhalten immer das Projektteam, das am besten zu Ihnen und Ihren Zielen passt.

Wie können wir Sie unterstützen?

Business Development
Founder and CEO
Business Development
Head of Operations
Business Development
Head of Business
Development
Business Development
Business Development
Operations and Project Management
Human Resources Management
Operations and Project Management
Medical Software, Verification and Regulatory Affairs
Operations and Project Management
Head of IVD
Operations and Project Management
Operations and
Project Management
Regulatory Affairs andTechnical Documentation IVD
Verification and
Regulatory Affairs
Regulatory Affairs andTechnical Documentation IVD
Quality Management and
Technical Documentation
Regulatory Affairs andTechnical Documentation IVD
Clinical Affairs
Regulatory Affairs andTechnical Documentation IVD
Regulatory Affairs and
Technical Documentation IVD
Technical Documentation and Regulatory Affairs
Quality Management and
Technical Documentation
Technical Documentation and Regulatory Affairs
Operations and
Business Development
Technical Documentation and Regulatory Affairs
Clinical Affairs and
Biological Safety
Technical Documentation and Regulatory Affairs
Technical Documentation and Regulatory Affairs
Project Management
Head of Clinical Affairs
Project Management
Quality Management Systems, Auditing
Project Management
Technical Documentation and
Regulatory Affairs
Project Management
Project Management
Technical Documentation and Regulatory Affairs
Verification, Testautomation
Technical Documentation and Regulatory Affairs
Regulatory Affairs
Technical Documentation and Regulatory Affairs
Regulatory Affairs and
Technical Documentation
Technical Documentation and Regulatory Affairs
Technical Documentation and
Regulatory Affairs
Regulatory Affairs and Biological Safety
Medical Software
Regulatory Affairs and Biological Safety
Technical Documentation and Regulatory Affairs
Regulatory Affairs and Biological Safety
Technical Documentation and Clinical Affairs
Regulatory Affairs and Biological Safety
Regulatory Affairs and Biological Safety
Quality Management and Technical Documentation
Regulatory Affairs
Quality Management and Technical Documentation
Regulatory Affairs and Technical Documentation
Quality Management and Technical Documentation
Clinical Affairs and
Technical Documentation
Quality Management and Technical Documentation
Quality Management and Technical Documentation
Business Development
Regulatory Affairs and Technical Documentation
Business Development
Clinical Affairs and
Technical Documentation
Business Development
Verification and
Technical Documentation
Business Development
Business Development
Administration
Marketing and Communications