Director, Development and Human Factor Engineering

Responsibilities:

• Manage and execute the company’s Design Controls and Drug Development Program
• Lead and responsible for human factor engineering activities
• Manage project and program budgets and timelines effectively

Qualifications:

• Bachelors, Masters, or PhD in a technical field related to Product Development or Industrialization
• Minimum 10+ years of medical device development experience, with experience in managing external CMO’s
• Minimum 5+ years of managing human factor engineering studies

Skills:

• Self-motivated and confident with excellent personnel management skills
• Strong analytical skills with the ability to creatively solve complex problems
• Excellent verbal and written communication skills