Associate Director, Human Factors Design And Development

CSL Behring

Not specified; not specified; competitive compensa...
8-12 years human factors experience
Medical device development background
Formative and summative usability studies
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 diverse teams including Clinical, Regulatory, Quality, and Manufacturing.

Matching Summary

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

Salary

Not specified; Not specified; Competitive compensation and benefits including flexible working arrangements

Skills & Requirements

Must-have

  • 8-12 years human factors experience
  • Medical device development background
  • Formative and summative usability studies
  • IEC 62366 and ISO 14971 knowledge
  • FDA and EU MDR regulatory submissions

Nice-to-have

  • Mentoring junior staff members
  • Global strategy leadership skills
  • Cross-functional team collaboration
  • Innovation and quality culture
  • Flexible working arrangements

Key Requirements

  • Master's or PhD in Human Factors or related field
  • 8-12 years experience in human factors engineering
  • Proven experience with medical device usability studies
  • Expertise in IEC 62366 and FDA guidance
  • Strong understanding of design controls and risk management

Work Rights

Not specified

Tailored Resume

Cover Letter