Qualitätsmanager/in
Core
Ensuring quality management compliance, documentation, and continuous improvement for medical device processes.
Role type
Quality Management Specialist (Medical Devices)
Domain
Medical Devices / Regulatory Compliance
Deliverable
dashboards & analysis
Required skills
ISO 9001, ISO 13485, MDR, ISO 14971, Risk Management, Internal Auditing, CAPA, Process Documentation
Preferred skills
Microsoft Office, Industry-specific Quality Software, English language skills
Responsibilities
Creating and updating quality management documents, conducting internal audits, participating in CAPA activities, managing risk assessments and FMEAs, planning and delivering quality training sessions.