Production Manager – Medical Devices, Lean & Compliance

UroMems

Fontanil-Cornillon

Sur place

EUR 90 000 - 130 000

Plein temps

Il y a 4 jours
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Résumé du poste

UroMems in Fontanil-Cornillon, FR, seeks a Production Manager to lead manufacturing of implantable medical devices, ensuring safety, quality, and compliant operations. You will own shop-floor execution, drive continuous improvement, manage a cross-functional team, and partner with Industrialization, Quality, and Regulatory Affairs to scale production up.

The role requires 10+ years in manufacturing with at least 3 years of people management, knowledge of ISO 13485, and experience in regulated

Qualifications

  • 10 years minimum experience in manufacturing, production engineering, or operations.
  • Minimum 3 years of people management experience.
  • Experience in regulated medical devices or similar environment.
  • Strong knowledge of ISO 13485 and regulatory manufacturing requirements.
  • Experience with audits, CAPA, and controlled documentation.

Responsabilités

  • Lead daily production execution and translate the plan into priorities.
  • Ensure compliance with ISO 13485 and regulatory requirements; prepare for audits.
  • Define training needs and develop the production team with HR, Quality, and process owners.
  • Monitor KPIs for safety, quality, delivery, and productivity; drive continuous improvement.

Connaissances

Team leadership
Lean manufacturing
Problem solving
Quality mindset

Formation

Engineering degree
Lean/Six Sigma

Outils

ERP/MRP
MES
Digital manufacturing

Description du poste

UroMems in Fontanil-Cornillon, FR, seeks a Production Manager to lead manufacturing of implantable medical devices, ensuring safety, quality, and compliant operations. You will own shop-floor execution, drive continuous improvement, manage a cross-functional team, and partner with Industrialization, Quality, and Regulatory Affairs to scale production up.

The role requires 10+ years in manufacturing with at least 3 years of people management, knowledge of ISO 13485, and experience in regulated

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