Senior QMS Lead, Medical Devices Quality & Compliance

Michael Page; Viseu; On-site; EUR 60,000 - 80,000; Full time

Job summary

Michael Page seeks an experienced Quality Manager to lead the QMS in a regulated medical device manufacturing environment. You will ensure regulatory and customer compliance, drive continuous improvement, and serve as the authority on product quality, patient safety, and regulatory compliance.

You will manage KPIs, audits, CAPA, risk management, and supplier/auditor interactions while guiding a quality team through process validation, product quality and patient safety considerations.

Qualifications

• Experience leading QMS in regulated medical device manufacturing (ISO 13485, MDSAP) and familiarity withQuality Management System elements.
• Strong knowledge of regulatory compliance and patient safety requirements.

Responsibilities

• Lead the QMS in a regulated medical device manufacturing environment and drive continuous improvement.
• Manage KPIs, audits, CAPA, risk management, and supplier/auditor interactions.
• Guide a quality team through process validation, product quality, and regulatory compliance to ensure customer satisfaction.

Job description

Michael Page seeks an experienced Quality Manager to lead the QMS in a regulated medical device manufacturing environment. You will ensure regulatory and customer compliance, drive continuous improvement, and serve as the authority on product quality, patient safety, and regulatory compliance.

You will manage KPIs, audits, CAPA, risk management, and supplier/auditor interactions while guiding a quality team through process validation, product quality and patient safety considerations.