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Business Process Manager Verification & DFM(m/w/x)
Description
In this role, you will drive process excellence by designing and improving business processes for product verification and manufacturability. By collaborating with cross-functional teams, you will ensure compliance and enhance product quality throughout the development lifecycle.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •5+ years of relevant experience in process management within the medical device or pharmaceutical industry
- •Strong knowledge of product development, verification processes, design controls, and DFM principles
- •Excellent strategic thinking, problem-solving, and analytical capabilities
- •Ability to influence and communicate effectively across all organizational levels
- •Ability to work in a fast-paced, global environment with multiple priorities
- •Bachelor’s or Master’s degree in Engineering, Quality Management, Industrial Engineering or related field
- •Fluency in English
- •Familiarity with PLM systems and digital documentation workflows
- •Experience applying agile methodologies in process design
- •Certification in Lean Six Sigma, Process Management or Project Management is a plus
- •Training in DFM methodologies and verification standards preferred
- •Experience with ISO 13485, FDA regulations, or similar compliance frameworks
- •German skills are a plus
Education
Work Experience
5 years
Tasks
- •Design and implement end-to-end business processes for Design Verification and DFM
- •Continuously improve processes related to Design, Risk Management, Testing, and Manufacturing Readiness
- •Ensure compliance with regulatory and quality standards throughout the product lifecycle
- •Collaborate with R&D, Quality, Regulatory, Manufacturing Engineering, Operations, and IT to harmonize processes
- •Develop and maintain process documentation, including Work Instructions, Templates, and Guidelines
- •Create training materials to ensure compliance with medical standards and company QMS
- •Conduct workshops and training sessions to identify process gaps and support change management
- •Translate business needs into functional solutions with system architects for PLM implementation
- •Monitor process performance and report KPIs to drive continuous improvement
- •Collect user feedback to enhance process efficiency
Tools & Technologies
Languages
English – Business Fluent
German – Basic
Benefits
Flexible Working
- •Flexible hours
- •Hybrid working policy
Diverse Work
- •Challenging assignments
Informal Culture
- •Multicultural team
- •Inclusive and collaborative environment
Modern Office
- •Modern working environment
- •State-of-the-art facilities
Other Benefits
- •Personal and professional development
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Business Process Manager Verification & DFM(m/w/x)
The AI Job Search Engine
Description
In this role, you will drive process excellence by designing and improving business processes for product verification and manufacturability. By collaborating with cross-functional teams, you will ensure compliance and enhance product quality throughout the development lifecycle.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •5+ years of relevant experience in process management within the medical device or pharmaceutical industry
- •Strong knowledge of product development, verification processes, design controls, and DFM principles
- •Excellent strategic thinking, problem-solving, and analytical capabilities
- •Ability to influence and communicate effectively across all organizational levels
- •Ability to work in a fast-paced, global environment with multiple priorities
- •Bachelor’s or Master’s degree in Engineering, Quality Management, Industrial Engineering or related field
- •Fluency in English
- •Familiarity with PLM systems and digital documentation workflows
- •Experience applying agile methodologies in process design
- •Certification in Lean Six Sigma, Process Management or Project Management is a plus
- •Training in DFM methodologies and verification standards preferred
- •Experience with ISO 13485, FDA regulations, or similar compliance frameworks
- •German skills are a plus
Education
Work Experience
5 years
Tasks
- •Design and implement end-to-end business processes for Design Verification and DFM
- •Continuously improve processes related to Design, Risk Management, Testing, and Manufacturing Readiness
- •Ensure compliance with regulatory and quality standards throughout the product lifecycle
- •Collaborate with R&D, Quality, Regulatory, Manufacturing Engineering, Operations, and IT to harmonize processes
- •Develop and maintain process documentation, including Work Instructions, Templates, and Guidelines
- •Create training materials to ensure compliance with medical standards and company QMS
- •Conduct workshops and training sessions to identify process gaps and support change management
- •Translate business needs into functional solutions with system architects for PLM implementation
- •Monitor process performance and report KPIs to drive continuous improvement
- •Collect user feedback to enhance process efficiency
Tools & Technologies
Languages
English – Business Fluent
German – Basic
Benefits
Flexible Working
- •Flexible hours
- •Hybrid working policy
Diverse Work
- •Challenging assignments
Informal Culture
- •Multicultural team
- •Inclusive and collaborative environment
Modern Office
- •Modern working environment
- •State-of-the-art facilities
Other Benefits
- •Personal and professional development
About the Company
SHL Medical
Industry
Healthcare
Description
Das Unternehmen ist ein weltweit führender Anbieter im Design, der Entwicklung und der Herstellung fortschrittlicher Selbstinjektionsgeräte.
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