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Senior Verification Engineer(m/w/x)
Description
As a Senior Verification Engineer, you will be at the forefront of developing verification strategies for innovative medical devices, collaborating with diverse teams, and mentoring junior engineers while ensuring compliance with regulatory standards.
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Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Master’s degree in medical engineering, software engineering, or related technical field
- •Several years of experience in software and system verification, preferably in medical device industry
- •Proven experience in test design, execution, and anomaly reporting
- •Test bench or fixture design, maintenance, improvement, and extension
- •Strong analytical, conceptual, and problem-solving skills
- •High documentation standards for V&V documentation aligned with regulatory standards
- •Hands-on experience with automated requirements and test management tools
- •Proficiency in test automation tools and scripting
- •Experience with CAN-Bus communication and Vector tools
- •Familiarity with regulatory standards such as IEC 60601-1, IEC 62304, and 510(k) submissions
- •Excellent communication skills in English; German is a strong plus
- •Self-motivated, proactive, and capable of working independently and in teams
Education
Work Experience
approx. 4 - 6 years
Tasks
- •Develop and implement verification strategies for medical devices
- •Lead the creation and optimization of test cases and verification protocols
- •Design and develop test fixtures and benches for testing
- •Drive the integration of test automation frameworks and tools
- •Create and manage detailed verification schedules
- •Perform statistical analysis and test method validation
- •Collaborate with cross-functional teams for risk and safety mitigation
- •Provide technical leadership and mentorship to junior engineers
- •Coordinate verification activities across multiple teams
- •Contribute to documentation for regulatory submissions
- •Support the evolution of the V&V framework and best practices
Tools & Technologies
Languages
English – Business Fluent
German – Basic
Benefits
Other Benefits
- •Supportive and inclusive environment
- •Exposure to advanced medical device development
- •Recognition through STARS Program
Informal Culture
- •Collaborative environment
Career Advancement
- •Professional career growth
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Senior Verification Engineer(m/w/x)
The AI Job Search Engine
Description
As a Senior Verification Engineer, you will be at the forefront of developing verification strategies for innovative medical devices, collaborating with diverse teams, and mentoring junior engineers while ensuring compliance with regulatory standards.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Master’s degree in medical engineering, software engineering, or related technical field
- •Several years of experience in software and system verification, preferably in medical device industry
- •Proven experience in test design, execution, and anomaly reporting
- •Test bench or fixture design, maintenance, improvement, and extension
- •Strong analytical, conceptual, and problem-solving skills
- •High documentation standards for V&V documentation aligned with regulatory standards
- •Hands-on experience with automated requirements and test management tools
- •Proficiency in test automation tools and scripting
- •Experience with CAN-Bus communication and Vector tools
- •Familiarity with regulatory standards such as IEC 60601-1, IEC 62304, and 510(k) submissions
- •Excellent communication skills in English; German is a strong plus
- •Self-motivated, proactive, and capable of working independently and in teams
Education
Work Experience
approx. 4 - 6 years
Tasks
- •Develop and implement verification strategies for medical devices
- •Lead the creation and optimization of test cases and verification protocols
- •Design and develop test fixtures and benches for testing
- •Drive the integration of test automation frameworks and tools
- •Create and manage detailed verification schedules
- •Perform statistical analysis and test method validation
- •Collaborate with cross-functional teams for risk and safety mitigation
- •Provide technical leadership and mentorship to junior engineers
- •Coordinate verification activities across multiple teams
- •Contribute to documentation for regulatory submissions
- •Support the evolution of the V&V framework and best practices
Tools & Technologies
Languages
English – Business Fluent
German – Basic
Benefits
Other Benefits
- •Supportive and inclusive environment
- •Exposure to advanced medical device development
- •Recognition through STARS Program
Informal Culture
- •Collaborative environment
Career Advancement
- •Professional career growth
About the Company
LivaNova Deutschland GmbH
Industry
Healthcare
Description
The company focuses on developing innovative medical technologies to improve patient outcomes.
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