Director of Quality Operations (m/f/d) - Hybrid

Artivion EMEA; Hechingen; Hybrid; EUR 120.000 - 160.000; Vollzeit

Benefits dieser Stelle

Hybrid-Arbeit

Dienstfahrrad

Firmenwagen

Betriebliche Altersvorsorge

Cafeteria Zuschuss

Zusammenfassung

JOTEC GmbH, eine hundertprozentige Tochtergesellschaft von Artivion, Inc., sucht eine/n Director of Quality Operations (m/w/d) – Hybrid in der Region Hechingen. Sie leiten Qualitäts- und Fertigungsprozesse und sorgen für compliant operations.

Sie verfügen über langjährige Führungsverantwortung im Qualitätsmanagement, fundierte FDA-/ISO-Kenntnisse und eine pragmatische, aber regelkonforme Arbeitsweise. Ihr Beitrag stärkt das Qualitätsnetzwerk weltweit.

Qualifikationen

• Mindestens 10 Jahre Qualitätserfahrung in der Fertigungsindustrie.
• Erfahrung in Qualitätsbetriebsführung, Herstellungsqualität und Validierung von Prozessen.
• Gute Kenntnisse von FDA-Regularien, ISO 13485 und weiteren relevanten Standards.

Aufgaben

• Überwachung von Fertigungssteuerung, Qualitätskontrolle und Qualitätslabor.
• Freigabe von Produkten auf dem Markt.
• Qualifikation von Anlagen, Validierung von Prozessen, Change-Control.
• Sicherung eines robusten Produktlebenszyklusmanagements.
• Festlegung und Überwachung von KPIs.
• Zusammenarbeit funktionsübergreifend.

Jobbeschreibung

• Jotec GmbH Jobportal
• Hechingen
• Kundenbetreuung, Hotline
• Publiziert: 10.09.2026

It’s a good feeling to know you're doing your best with purpose every day. At Artivion, we manufacture high-quality products and solutions for the treatment of aortic diseases. Together with surgeons worldwide, we save lives. In doing so, we rely on the strengths of each and every employee. Your strength counts, too: As an important link in the chain, you make a contribution to saving lives together with us. Contribute your strengths and let us grow together. We are hiring a

Director of Quality Operations (m/f/d) - Hybrid

Your Strength

• 10+ years of experience in quality management in a manufacturing organization within the medical industry
• Focus of experience on Quality Operations/Manufacturing
• Extensive knowledge of FDA regulations, ISO 13485, and other relevant quality standards
• Proven leadership experience in quality control, manufacturing quality, and process validation
• Strong analytical, problem-solving, and decision-making abilities
• Excellent communication, interpersonal, and team leadership skills
• Experience in managing audits, regulatory inspections, and compliance initiatives in the Operations-Field
• Pragmatic, but compliant approach

Your Contribution

• Oversee manufacturing control, quality control, quality engineering, and quality laboratory operations to ensure compliance with FDA, ISO, MDR, and other applicable regulations
• Release of products to the markets
• Lead qualification of equipment, verification and validation of processes, and change control activities
• Ensure robust product lifecycle management
• Establish and monitor key performance indicators
• Support change control for sustaining business
• Drive effective problem solving, error proofing, and process improvements
• Streamline quality processes to enable efficiencies and overall process effectiveness
• Develop and mentor the sustain quality team, fostering a culture of quality awareness and operational excellence
• Collaborate cross-functionally
• Serve as the primary point of contact for quality-related communications with internal stakeholders, regulatory authorities, and external customers

Our Strength

• An exciting field of activity in a global team
• An independent area of responsibility
• Intensive training with mentoring program
• Various benefits such as hybrid working, business bike, company car, company pension and subsidy for our canteen

Contact

Maximiljane Tyrs, T: 07471 922 352

JOTEC GmbH, a wholly owned subsidiary of Artivion, Inc.,

Lotzenäcker 23, 72379 Hechingen

www.artivion.com