Associate Director, Human Factors Design And Development

CSL Behring

Not specified; competitive compensation + benefits...
Human factors engineering expertise
Formative and summative usability studies
Iso 14971 risk management knowledge
This role leads the integration of human factors engineering to ensure medical products are safe, effective, and user-friendly

Job Summary

  • This role leads the integration of human factors engineering to ensure medical products are safe, effective, and user-friendly.
  • The position requires conducting formative and summative usability studies while preparing HF-related sections for global regulatory submissions.
  • Candidates will mentor junior staff and collaborate with cross-functional teams including Clinical, Regulatory, and Quality departments.

Matching Summary

This role leads the integration of human factors engineering to ensure medical products are safe, effective, and user-friendly.

Salary

Not specified; Competitive compensation and benefits; Flexible working arrangements included

Skills & Requirements

Must-have

  • Human Factors Engineering expertise
  • Formative and Summative Usability Studies
  • ISO 14971 Risk Management knowledge
  • IEC 62366 Standard application
  • FDA and EU MDR Regulatory submissions

Nice-to-have

  • Cross-functional team leadership skills
  • Mentoring junior staff experience
  • Global strategy development capability
  • Strong written communication skills

Key Requirements

  • Master's or PhD in Human Factors or related field
  • 8-12 years of experience in human factors engineering
  • Experience with medical device design controls

Work Rights

Not specified

Tailored Resume

Cover Letter