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Senior Verification Engineer(m/w/x)
Description
In this role, you will ensure the quality and safety of innovative medical and biological consumables by planning and conducting verification processes, collaborating with diverse teams, and preparing essential technical documentation.
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 or equivalent in engineering, life sciences, medical technology, or comparable field
- •Professional experience in verification, ideally in medical technology, biotechnology, or related field
- •Familiarity with regulated environments (e.g., ISO 13485, FDA 21 CFR) and structured, solution-oriented working style
- •Analytical and well-organized with strong problem-solving skills
- •Solid English skills, both written and spoken
Education
Work Experience
approx. 4 - 6 years
Tasks
- •Plan, conduct, and document verification processes
- •Develop test strategies and methods
- •Collaborate with interdisciplinary teams to validate testing procedures
- •Analyze test results and identify optimization potential
- •Prepare technical documentation in compliance with regulatory standards
Languages
English – Business Fluent
Benefits
Flexible Working
- •Flexible and remote work
Team Events
- •Wide range of corporate sports activities
Learning & Development
- •In-house training academy
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Senior Verification Engineer(m/w/x)
The AI Job Search Engine
Description
In this role, you will ensure the quality and safety of innovative medical and biological consumables by planning and conducting verification processes, collaborating with diverse teams, and preparing essential technical documentation.
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 or equivalent in engineering, life sciences, medical technology, or comparable field
- •Professional experience in verification, ideally in medical technology, biotechnology, or related field
- •Familiarity with regulated environments (e.g., ISO 13485, FDA 21 CFR) and structured, solution-oriented working style
- •Analytical and well-organized with strong problem-solving skills
- •Solid English skills, both written and spoken
Education
Work Experience
approx. 4 - 6 years
Tasks
- •Plan, conduct, and document verification processes
- •Develop test strategies and methods
- •Collaborate with interdisciplinary teams to validate testing procedures
- •Analyze test results and identify optimization potential
- •Prepare technical documentation in compliance with regulatory standards
Languages
English – Business Fluent
Benefits
Flexible Working
- •Flexible and remote work
Team Events
- •Wide range of corporate sports activities
Learning & Development
- •In-house training academy
About the Company
Miltenyi Biotec
Industry
Other
Description
Das Unternehmen entwickelt einzigartige Lösungen für die biomedizinische Spitzenforschung sowie neuartige Zell- und Gentherapien.
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