Mitarbeiter für Qualitätssicherung/ Regulatory Affairs Onsite (w/m/d)
On-site
Core
Quality Assurance and Regulatory Affairs specialist for medical devices, responsible for documentation, quality management, product testing, and supplier management.
Role type
Quality Assurance and Regulatory Affairs Specialist
Builds
Medical device documentation and quality management systems
Domain
Medical Devices / Healthcare
Required skills
Medical device knowledge, Quality Management Systems (QMS), Regulatory Affairs, Documentation, Product testing, Supplier management, MS Office
Preferred skills
Natural sciences or medical-technical degree, Teamwork, German C2, English C1
Responsibilities
Create and maintain product documentation, Create and maintain QM handbook, Conduct product tests, Manage suppliers
Seniority
Entry to Mid-level