Madrid-Based Global Supplier Quality Manager

Institut Straumann AG; Madrid; Presencial; EUR 70.000 - 100.000; Jornada completa

Descripción de la vacante

Straumann Group in Madrid (Spain) is hiring a Supplier Quality Manager to lead the supplier quality management function and ensure compliance, quality, and supplier performance across the global Straumann Group.

The role involves managing audits, supplier qualifications, and quality systems compliance in a highly regulated medical device environment, with collaboration across internal and external stakeholders.

Formación

• University degree in Quality Management, Engineering, Life Sciences, Pharmacy, Medicine, Law or a comparable discipline.
• Proven and strong professional experience in Quality Management, preferably within the medical device industry or pharma.
• Proven experience in Supplier Quality Management and supplier qualification processes.
• Strong knowledge of ISO 13485, MDR 2017/745, MDD 93/42/EEC, FDA 21 CFR 820 (QMSR), and related quality systems.

Responsabilidades

• Managing supplier onboarding, qualification, and monitoring processes.
• Defining and implementing supplier compliance strategies in collaboration with Procurement and other stakeholders.
• Establishing and maintaining Quality Assurance Agreements with suppliers, subsidiaries, and distributors.
• Monitoring supplier performance through KPIs and continuous improvement initiatives.
• Leading and developing the Supplier Quality Management team.

Conocimientos

Fluent English

Leadership

Lean Management Experience

Educación

Quality Management / Engineering degree

ISO 13485 Auditor Training

Herramientas

SAP

e-QMS systems

MS Office

Document control systems

Descripción del empleo

Straumann Group in Madrid (Spain) is hiring a Supplier Quality Manager to lead the supplier quality management function and ensure compliance, quality, and supplier performance across the global Straumann Group.

The role involves managing audits, supplier qualifications, and quality systems compliance in a highly regulated medical device environment, with collaboration across internal and external stakeholders.