CSL Behring
Senior Principal Engineer, Human Factors(m/w/x)
Full-timeOn-siteSenior
Bern
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CSCSL Behring
Associate Director, Human Factors Design and Development(m/w/x)
Bern
Full-timeOn-siteSenior
Nejo AI Summary
Developing global human factors strategies for biotherapeutics, identifying user risks and integrating HF early in design. 8-12 years of medical device HF experience required. Flexible working arrangements, company car for private use.
Requirements
- Master’s or PhD in Human Factors, Industrial Design, HCI, Ergonomics, or Biomedical Engineering
- 8–12 years of human factors engineering, usability, or product development experience
- Medical devices, combination products, or healthcare technologies experience
- Proven experience conducting formative and summative usability studies
- Knowledge of human factors standards (IEC 62366, FDA guidance, ISO 14971)
- Expertise in human factors and usability engineering
- Strong understanding of design controls and risk management
- Usability study design, execution, and analysis experience
- Regulatory knowledge for HF submissions and compliance
- Cross-functional collaboration and project leadership
- Excellent written and verbal communication skills
Tasks
- Develop global human factors strategies
- Identify critical user interactions and risks
- Integrate human factors early in design
- Lead human factors design inputs and controls
- Guide interface design and user instructions
- Collaborate with R&D and Engineering teams
- Conduct human factors risk assessments
- Plan and execute usability studies
- Analyze study data for design improvements
- Document usability validation for regulatory submissions
- Support HF-related regulatory submissions
- Ensure compliance with international standards
- Serve as HF expert for regulatory inspections
- Partner with cross-functional teams
- Mentor junior human factors staff
- Participate in project planning and reviews
- Attend senior leadership meetings
Work Experience
- 8 - 12 years
Education
- Master's degree
Languages
- English – Business Fluent
Benefits
Flexible Working
- Flexible working arrangements
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of CSL Behring and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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CSCSL Behring
Associate Director, Human Factors Design and Development(m/w/x)
Bern
Full-timeOn-siteSenior
Nejo AI Summary
Developing global human factors strategies for biotherapeutics, identifying user risks and integrating HF early in design. 8-12 years of medical device HF experience required. Flexible working arrangements, company car for private use.
Requirements
- Master’s or PhD in Human Factors, Industrial Design, HCI, Ergonomics, or Biomedical Engineering
- 8–12 years of human factors engineering, usability, or product development experience
- Medical devices, combination products, or healthcare technologies experience
- Proven experience conducting formative and summative usability studies
- Knowledge of human factors standards (IEC 62366, FDA guidance, ISO 14971)
- Expertise in human factors and usability engineering
- Strong understanding of design controls and risk management
- Usability study design, execution, and analysis experience
- Regulatory knowledge for HF submissions and compliance
- Cross-functional collaboration and project leadership
- Excellent written and verbal communication skills
Tasks
- Develop global human factors strategies
- Identify critical user interactions and risks
- Integrate human factors early in design
- Lead human factors design inputs and controls
- Guide interface design and user instructions
- Collaborate with R&D and Engineering teams
- Conduct human factors risk assessments
- Plan and execute usability studies
- Analyze study data for design improvements
- Document usability validation for regulatory submissions
- Support HF-related regulatory submissions
- Ensure compliance with international standards
- Serve as HF expert for regulatory inspections
- Partner with cross-functional teams
- Mentor junior human factors staff
- Participate in project planning and reviews
- Attend senior leadership meetings
Work Experience
- 8 - 12 years
Education
- Master's degree
Languages
- English – Business Fluent
Benefits
Flexible Working
- Flexible working arrangements
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of CSL Behring and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
About the Company
CSL Behring
Industry
Pharmaceuticals
Description
Das Unternehmen ist ein globaler Marktführer in der Biotherapeutik, der innovative Therapien für Patienten mit immunologischen, hämatologischen, kardiovaskulären und anderen Erkrankungen entwickelt.
Not a perfect match?
- CSL Behring
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