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Quality & Regulatory Affairs Lead – Medical Device Software (SaMD/SiMD)(m/w/x)
Beschreibung
In this hands-on leadership role, you will shape regulatory strategy for medical device software while building a dedicated team and ensuring products meet the highest global standards.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
Anforderungen
- •Experience in quality management and regulatory affairs
- •Knowledge of ISO 13485, MDR, and FDA
- •Experience coordinating audits with external auditors
- •Hands-on execution and pragmatic leadership skills
- •Ownership of complex end-to-end projects
- •Strong communication and professional confidence
- •Motivation to build quality organizations
Ausbildung
Berufserfahrung
2 - 5 Jahre
Aufgaben
- •Define regulatory strategies for SaMD and SiMD projects
- •Ensure compliance with MDR and FDA expectations
- •Guide documentation for interventional planning software
- •Maintain and improve the ISO 13485 QMS
- •Implement quality policies and monitor KPIs
- •Coordinate internal and external audits
- •Assess the impact of regulatory changes
- •Promote a company-wide culture of compliance
- •Support business development and project scoping
- •Hire and mentor the Quality Management team
- •Execute hands-on documentation and compliance work
Tools & Technologien
Sprachen
Englisch – verhandlungssicher
Benefits
Firmenfahrrad
- •Bike leasing
Gesundheits- & Fitnessangebote
- •Sports programs
Öffi Tickets
- •Deutschlandticket
Team Events & Ausflüge
- •Team events
- •Summer party
- •Oktoberfest
- LivaNova Deutschland GmbHVollzeitnur vor OrtSeniorMünchen
- MED CARE VISIONS® GmbH
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Vollzeitnur vor OrtSeniorMünchen
Quality & Regulatory Affairs Lead – Medical Device Software (SaMD/SiMD)(m/w/x)
Die KI-Suchmaschine für Jobs
Beschreibung
In this hands-on leadership role, you will shape regulatory strategy for medical device software while building a dedicated team and ensuring products meet the highest global standards.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
Anforderungen
- •Experience in quality management and regulatory affairs
- •Knowledge of ISO 13485, MDR, and FDA
- •Experience coordinating audits with external auditors
- •Hands-on execution and pragmatic leadership skills
- •Ownership of complex end-to-end projects
- •Strong communication and professional confidence
- •Motivation to build quality organizations
Ausbildung
Berufserfahrung
2 - 5 Jahre
Aufgaben
- •Define regulatory strategies for SaMD and SiMD projects
- •Ensure compliance with MDR and FDA expectations
- •Guide documentation for interventional planning software
- •Maintain and improve the ISO 13485 QMS
- •Implement quality policies and monitor KPIs
- •Coordinate internal and external audits
- •Assess the impact of regulatory changes
- •Promote a company-wide culture of compliance
- •Support business development and project scoping
- •Hire and mentor the Quality Management team
- •Execute hands-on documentation and compliance work
Tools & Technologien
Sprachen
Englisch – verhandlungssicher
Benefits
Firmenfahrrad
- •Bike leasing
Gesundheits- & Fitnessangebote
- •Sports programs
Öffi Tickets
- •Deutschlandticket
Team Events & Ausflüge
- •Team events
- •Summer party
- •Oktoberfest
Über das Unternehmen
ImFusion GmbH
Branche
Healthcare
Beschreibung
The company is a R&D consulting firm specializing in medical imaging technologies, AI, and robotics.
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