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Director of Procurement

KARDION

Remote
Remote Senior 🇬🇧 English
EU MDR ISO 13485 FDA QSR

Job description

About the role

Kardion, a fast‑growing medical device company, is seeking a Director of Procurement to lead its global sourcing, supplier management and contract manufacturing operations. This senior, operationally focused position will shape a scalable procurement strategy that supports commercialization goals while ensuring compliance with regulatory standards.

Key responsibilities

  • Lead, mentor and develop a team of six buyers covering direct, indirect and NPI procurement categories.
  • Design and strengthen sourcing strategies for components, materials, tooling and services.
  • Own the full supplier lifecycle: selection, qualification, onboarding and performance management.
  • Negotiate contracts, pricing and commercial terms to meet cost, quality and risk‑mitigation objectives.
  • Serve as the primary operational interface for external manufacturing partners in Germany and other regions.
  • Oversee capacity planning, production scheduling and issue resolution with CMOs.
  • Support technology transfer, scale‑up and validation activities alongside Engineering and Quality teams.
  • Establish supplier governance frameworks, KPIs and performance review mechanisms.
  • Ensure supplier compliance with ISO 13485, EU MDR, FDA QSR and internal quality requirements.
  • Lead supplier audits, corrective actions and risk‑mitigation initiatives.
  • Maintain supplier risk assessments and business continuity plans.
  • Partner cross‑functionally with Engineering, Quality, Regulatory and Finance to align procurement strategies with product development milestones.

Required profile

  • Bachelor’s degree in Supply Chain, Engineering, Business or a related field.
  • 6–10 years of procurement and supplier management experience in MedTech, biotech or another regulated manufacturing environment.
  • Demonstrated experience managing contract manufacturing organizations and leading cross‑functional sourcing initiatives.
  • Working knowledge of EU MDR, ISO 13485 and FDA QSR regulations.

Required skills

  • EU MDR
  • ISO 13485
  • FDA QSR

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Published 3 months ago

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KARDION