Mitarbeiter:in (m/w/d) im Qualitätsmanagement (Sachbearbeitung - in Teilzeit)
Core
Ensuring high quality standards for medical products and processes through documentation management, specification verification, and supplier compliance checks.
Role type
Quality Management Specialist (Medical Devices)
Builds
Medical device products and processes
Domain
Medical Devices / Healthcare
Required skills
Documentation management, Specification verification, Supplier compliance checks, ERP system usage, Regulatory knowledge (ISO 13485, MDR), Sterilization certificate verification, Bioburden/Sterility test tracking, Cross-functional communication
Preferred skills
Medical device industry experience, Advanced Excel skills, Knowledge of European Medical Device Regulation (MDR)
Responsibilities
Verify and manage product specifications and supplier documents, Review new articles/suppliers via booking journal, Maintain QM documentation in ERP system, Check supplier conformity declarations, Support release of sterilized goods, Verify sterilization and batch certificates, Track missing quality documents
Seniority
Entry to Mid-level, Part-time