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Quality & Regulatory Affairs Lead – Medical Device Software (SaMD/SiMD)(m/w/x)
Description
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.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •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
Education
Work Experience
2 - 5 years
Tasks
- •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 & Technologies
Languages
English – Business Fluent
Benefits
Company Bike
- •Bike leasing
Healthcare & Fitness
- •Sports programs
Public Transport Subsidies
- •Deutschlandticket
Team Events
- •Team events
- •Summer party
- •Oktoberfest
- LivaNova Deutschland GmbHFull-timeOn-siteSeniorMünchen
- MED CARE VISIONS® GmbH
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Quality & Regulatory Affairs Lead – Medical Device Software (SaMD/SiMD)(m/w/x)
The AI Job Search Engine
Description
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.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •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
Education
Work Experience
2 - 5 years
Tasks
- •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 & Technologies
Languages
English – Business Fluent
Benefits
Company Bike
- •Bike leasing
Healthcare & Fitness
- •Sports programs
Public Transport Subsidies
- •Deutschlandticket
Team Events
- •Team events
- •Summer party
- •Oktoberfest
About the Company
ImFusion GmbH
Industry
Healthcare
Description
The company is a R&D consulting firm specializing in medical imaging technologies, AI, and robotics.
- LivaNova Deutschland GmbH
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