Qualitätsmanagement | Qualitätsingenieur | Auditor
- Verfügbarkeit einsehen
- 0 Referenzen
- 95‐115€/Stunde
- 81547 München
- DACH-Region
- de | en | es
- 14.04.2026
- Contract ready
Kurzvorstellung
Geschäftsdaten
Qualifikationen
Projekt‐ & Berufserfahrung
9/2024 – 11/2025
Tätigkeitsbeschreibung
Contributing to the design transfer process to and from suppliers
Ensuring compliance with internal and external requirements
Handling supplier audit management
Supporting the supplier selection process
Establishing and maintaining systems for supplier assessment, qualification, and ranking.
Handling supplier non-conformances
Implementing and maintaining processes for supplier management and continuous development.
Lieferantenmanagement (allg.), Qualitätsingenieur, Qualitätsmanager, Auditor
3/2023 – 9/2024
Tätigkeitsbeschreibung
Coordination of risk management activities
Supporting design transfer activities
Coordinating SOP updates due to regulatory requirements
Enforcement of corrective and preventive actions
Stoppage of non-conformities to assure safeness and effectiveness of the products
Handling of customer complaints
Preparing and updating of technical documentations
Supporting on/offsite audits
Coordinating biocompatibility evaluations
Qualitätsingenieur, Qualitätsmanager, Auditor
9/2019 – 2/2023
Tätigkeitsbeschreibung
Execution of change management procedures to improve production processes
Enforcement of corrective and preventive actions
Stoppage of non-conformities to assure safeness and effectiveness of the products
Handling of customer complaints including informing competent authorities and notified body
Qualification, coordination, control and management of suppliers
Implementing of QM-Processes according to regulatory requirements (MDSAP, 21CFR820)
Representation of Quality Management in product development activities
Qualitätsingenieur, Qualitätsmanager
12/2018 – 9/2019
TätigkeitsbeschreibungSupport of Quality Management activities
Eingesetzte QualifikationenQualitätsmitarbeiter
Zertifikate
TU Lübeck
Oncampus
DQS
Ausbildung
Hochschule Offenburg
Offenburg
Über mich
ISO 13485, ISO 14971, IEC 62304, IEC 60601, ISO 10993 standards implementation and compliance management
Supplier Management
Supplier audit management, selection processes, assessment, qualification, ranking and non-conformance handling
Process Control and Validation
Production process control, process validation and technical documentation management
Medical Device Sterilization
Sterilization processes for medical devices according to regulatory standards
MDR Compliance
Medical Device Regulation compliance and implementation
Project Management
Project coordination and management methodologies
Corrective and Preventive Actions
Enforcement of corrective and preventive actions, Stoppage of non-conformities to assure safeness and effectiveness of the products
Complaint Handling
Handling of customer complaints including informing competent authorities and notified body
Weitere Kenntnisse
Persönliche Daten
- Deutsch (Muttersprache)
- Englisch (Fließend)
- Spanisch (Grundkenntnisse)
- Europäische Union
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