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Human Factor Engineer

Job in Milan, Lombardy, Italy
Listing for: Altro
Full Time position
Listed on 2026-08-04
Job specializations:
  • Engineering
    Biomedical Engineer, Medical Device Industry, Quality Engineering, Systems Engineer
Salary/Wage Range or Industry Benchmark: 60000 - 90000 EUR Yearly EUR 60000.00 90000.00 YEAR
Job Description & How to Apply Below
In this role, you will shape the human factors strategy for medical products to optimize user experience and patient outcomes. You will collaborate with cross-functional teams to integrate HF into product design and lifecycle management, ensuring compliance with ISO, FDA and MDR requirements. You will lead external partners in HF studies and drive documentation from task analysis to final reports.

This position offers a chance to contribute to safer, user-centered medical devices in a dynamic, international environment.

5-8% variable bonus/MBO

private health insurance

pension fund

salary based on experience and internal equity

career progression and compensation reviews

Define user requirements and translate them into product solutions to improve user experience

Develop and own the Human Factors strategy and documentation for HF files

Coordinate and manage external partners conducting HF studies under a risk-based approach

Lead preparation of task analyses, formative and summative studies, usability risk assessments, HF plan and final reports

Ensure HF activities are integrated into design development from feasibility to lifecycle management

Apply design control principles and participate in activities like product risk management, requirements definition, testing (DVT), and equipment validation (IQ/OQ/PQ)

Degree in Biomedical Engineering, Design, HFE or related fields

1+ year of experience in HFE and medical product development

Knowledge of user-centered design and usability engineering

Experience generating HF usability documentation (URRA, usability study docs)

Strong collaboration with cross-functional teams (engineering, regulatory, quality, etc.)

Experience with all phases of medical device product development under a QMS

Knowledge of IEC 62366, FDA HFE guidelines, ISO 13485, ISO 14971, ISO 14971?

Design control guidance under FDA and MDR

In this role, you will shape the human factors strategy for medical products to optimize user experience and patient outcomes. You Will coll

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