27 mei 2026
Quality Manager - Medical Devices (TEMP)
| Branche | Zie onder |
| Dienstverband | Zie onder |
| Uren | Zie onder |
| Locatie | Zoetermeer |
| Opleidingsniveau | HBO / bachelor |
| Contactpersoon |
Olawale Olukunga +31622258890 |
Informatie
- Track and report KPI;
- Act as an escalation point, be a bridge between NMD and the suppliers;
- Support review of supplier quality issues to the organization related: to servicing data, data from complaint handling team, and others;
- Support selection and approval of supplier, alongside with C&P (Sourcing);
- Support engineering changes and projects, including product testing and validation documentation from suppliers;
- Assess supplier changes;
- Impact in product and processes;
- Support and manage ownership of supplier quality management processes within the QMS;
- Cross-functional collaboration;
- Support queries from stakeholders related to supplier quality;
- Ensure alignment between technical, quality, and business priorities.
Omschrijving
- Track and report KPI;
- Act as an escalation point, be a bridge between NMD and the suppliers;
- Support review of supplier quality issues to the organization related: to servicing data, data from complaint handling team, and others;
- Support selection and approval of supplier, alongside with C&P (Sourcing);
- Support engineering changes and projects, including product testing and validation documentation from suppliers;
- Assess supplier changes;
- Impact in product and processes;
- Support and manage ownership of supplier quality management processes within the QMS;
- Cross-functional collaboration;
- Support queries from stakeholders related to supplier quality;
- Ensure alignment between technical, quality, and business priorities.
Functie eisen
- 5+ Years of experience in Supplier Quality Management or Quality Engineering;
- Experienced in Medical Device manufacturing/processes or similar OR minimum 2-3 years in industries such as pharma, medical device or highly regulated industry. (i.e., automotive, aerospace);
- Knowledge of ISO 13485 and MDR;
- Engineering, bachelor preferred;
- Proof experience performing supplier quality audits;
- Role will be hybrid, Fast Learning Ability , Proactive and ownership and Strong communication skills.
