Part-Time Human Factors Specialist – Medical Devices

Addison Group; Schaumburg (IL); Hybrid; USD 82,656 - 96,432; Part time

Benefits offered by this job

Medical benefits

Dental benefits

Vision benefits

401(k) benefits

Job summary

Addison Group is seeking a part-time Human Factors Specialist based in Schaumburg, Illinois. This role supports usability engineering activities in a hybrid work environment, requiring occasional on-site participation for testing.

The ideal candidate will have 1–3 years of experience with usability studies, strong organizational and analytical skills, and proficiency in Microsoft Office. You'll assist in coordinating, executing, and reporting usability studies for medical devices within regulatory standards.

Qualifications

• 1–3 years of experience supporting usability studies or human factors activities.
• Strong organizational, analytical, and documentation skills.
• Proficiency with Microsoft Office Suite.
• Exposure to FDA Human Factors guidance or similar standards is a plus.

Responsibilities

• Support the execution of human factors and usability testing activities.
• Assist with formative and validation usability studies across projects.
• Coordinate study logistics including participant scheduling and session support.
• Act as a moderator or note-taker during study activities.
• Compile and analyze qualitative and quantitative study data.

Skills

Usability studies support

Organizational skills

Analytical skills

Documentation skills

Microsoft Office Suite proficiency

Job description

Addison Group is seeking a part-time Human Factors Specialist based in Schaumburg, Illinois. This role supports usability engineering activities in a hybrid work environment, requiring occasional on-site participation for testing.

The ideal candidate will have 1–3 years of experience with usability studies, strong organizational and analytical skills, and proficiency in Microsoft Office. You'll assist in coordinating, executing, and reporting usability studies for medical devices within regulatory standards.