Quality Assurance Manager

Certexe; Firenze; Remoto; EUR 50.000 - 70.000; Tempo pieno

Descrizione del lavoro

A newly founded Italian company is seeking an experienced Quality Manager to develop and manage their Quality Management System (QMS). This role involves working closely with the management team to achieve MDR accreditation and ensure long-term compliance with applicable standards. The position offers competitive compensation and an opportunity for growth within a start-up environment.

Servizi

Competitive compensation

Flexible working hours

Growth opportunities

Competenze

• Experience in developing and managing Quality Management Systems (QMS).
• Strong knowledge of ISO / IEC 17021, ISO / IEC 17065, and ISO / IEC 17020 standards.
• Ability to coordinate with technical teams for regulatory compliance.

Mansioni

• Lead the implementation and management of QMS.
• Work with the management team to secure initial MDR accreditation.
• Maintain and improve QMS for compliance with relevant standards.

Descrizione del lavoro

Overview

Position : Quality Manager – Medical Devices / Conformity Assessment Body

Location : Primarily remote (with regular coordination meetings on-site and / or online)

Type : Full-time

About Certexe

Certexe is a newly founded Italian company, headquartered in Italy, on the path to becoming a CE Notified Body under MDR and IVDR. Joining us now means stepping in at the foundation phase, where your expertise will be key to achieving accreditation and building the systems that will support long-term international growth. We offer competitive compensation, flexibility, and the rare opportunity to grow with a Notified Body from start-up to international recognition.

About the Role

We are seeking an experienced and highly motivated Quality Manager to lead the development, implementation, and management of our Quality Management System (QMS) in accordance with applicable standards and regulatory requirements. In this strategic role, you will work closely with the Technical Director, Deputy Technical Director, and the management team to secure our initial MDR accreditation. Once accreditation is achieved, you will be responsible for maintaining, improving, and expanding the QMS to ensure compliance with ISO / IEC 17021, ISO / IEC 17065, ISO / IEC 17020, and other relevant schemes.