Quality Manager

Thor Companies; Baden-Württemberg; Hybrid; EUR 70.000 - 90.000; Vollzeit

Zusammenfassung

A leading medical engineering firm is seeking an experienced Quality Manager to oversee quality initiatives and compliance within a collaborative environment in Stuttgart. The ideal candidate will have over 5 years of experience in quality assurance, particularly in the medical device industry, and a relevant degree. This hybrid role requires onsite presence three days a week, offering an excellent opportunity to drive innovation while ensuring operational excellence.

Qualifikationen

• Minimum 5 years in quality assurance or regulatory affairs in medical devices.
• Leadership experience is essential.
• Experience with Class II or III medical devices required.
• Certified auditor preferred.

Aufgaben

• Lead Quality initiatives including QMS evaluations.
• Define and monitor departmental goals.
• Manage core Quality Systems and documentation.
• Coach and develop the Quality team.
• Perform internal audits and external assessments.

Kenntnisse

Quality assurance

Regulatory affairs

Leadership

Ausbildung

Bachelor's degree in Engineering, Quality, Regulatory Affairs or related field

Tools

CAPA

ISO compliance

Jobbeschreibung

Overview

Thor Companies are supporting a global medical engineering and technology leader in their search for an experienced Quality Manager to join their innovation hub in Stuttgart. The company has built a reputation as a pioneer in advanced materials and manufacturing solutions, serving industrial and commercial markets worldwide. With a strong focus on sustainability and process excellence, they continue to drive innovation and growth while offering employees a collaborative, multicultural workplace.

Responsibilities

• Lead and drive Quality initiatives, including QMS evaluations and ongoing continuous improvement.


• Define and monitor departmental goals to uphold operational excellence.


• Manage core Quality Systems, such as CAPA, ISO compliance, non-conformance management, document control, supplier quality, customer feedback, and ITAR adherence.


• Allocate and coordinate resources for product evaluations and customer engagement.


• Ensure the maintenance and accuracy of documentation required under the Quality Management System.


• Coach and develop the Quality team, promoting a culture of continuous enhancement.


• Perform internal audits and serve as the Quality representative during external assessments.


• Support system integrations tied to acquisitions and the introduction of new manufacturing capabilities.

Qualifications

• A minimum of 5 years quality assurance and/or regulatory affairs experience in the medical device space


• Leadership/people management experience


• Experience with Class II or III medical devices


• Bachelor\'s degree in Engineering, Quality, Regulatory Affairs or related field


• Certified auditor

This is a hybrid role - onsite presence is expected 3 days per week.