Main responsibilities
* communicate and follow up on supplier evaluations and audits.
* coordinate the receipt and inspection of incoming materials, ensuring compliance with specifications.
* follow up on raw material specifications (rms).
* collaborate in supplier development and continuous improvement.
* monitor supplier performance indicators and report results.
* manage non-conforming material (mrb), rmas, and credit notes.
* analyze data to anticipate risks and improve the supply chain.
* participate in projects to optimize purchasing and quality processes.
* maintain effective communication with purchasing and production teams.
* promote a quality culture within the supply chain.
* participate on the production floor as process engineering support, ensuring compliance with specifications and quality controls.
* support process validation activities in a medical environment (iq, oq, pq), ensuring compliance with established requirements.
requirements
* bachelor's degree in industrial, quality, biomedical engineering, or related field.
* 1–3 years of experience in quality, processes, or production (preferably in medical or regulated industry).
* experience on the production floor.
* intermediate english (b1).
technical knowledge
* iso 13485
* raw material specifications (rms)
* non-conforming material management (mrb, rma)
* traceability and documentation
* manufacturing processes on the production floor
* process validation (iq, oq, pq)
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