Mitarbeiter für Qualitätssicherung / Regulatory Affairs Onsite (w/m/d)
On-site
Core
Quality Assurance and Regulatory Affairs specialist ensuring compliance and documentation for a medical device manufacturer's product portfolio.
Role type
Quality Assurance / Regulatory Affairs Specialist
Builds
Medical device products and documentation
Domain
Medical Devices / Healthcare
Required skills
Medical device knowledge, Quality Management Systems (QMS), Regulatory Affairs, Documentation management, Supplier management, MS Office / LibreOffice
Preferred skills
Natural sciences or medical-technical degree, Teamwork
Technologies
MS Office, LibreOffice
Responsibilities
Create and maintain product documentation, Maintain QM handbook, Conduct product tests, Manage suppliers
Seniority
Mid-level, hands-on IC