Note: The job is a remote job and is open to candidates in USA. ACL Digital is seeking a Medical Device Human Factors Engineer to support the development and improvement of drug delivery devices in compliance with industry regulations. The role involves collaborating with cross-functional teams to conduct human factors research, usability studies, and documentation to enhance product design and user experience.
Responsibilities
- Work collaboratively with HFE/UE, engineering, design, commercial, and product teams to ensure successful translation of user requirements into products, to create user interface (UI) requirements, that meet the needs of users and enrich the overall user experience across client’s portfolio or programs
- Supporting usability activities such as study planning/coordination/management, protocol development, study moderation, data collection, material development, IRB submissions, participant recruitment, data analysis, and HFE/UE design history file documentation to support project needs
- Collaborate with the HFE/UE lead to ensure Human-system capabilities and limitations are properly reflected in the system requirements, and HFE/UE input is provided across functions to develop product design, packaging, labeling, and training requirements
- Support appropriate human factors and usability engineering activities to improve the design of products, specifically the device-user interfaces, including the device, packaging, labeling, and instructions for use while minimizing the potential for use errors
- Analyze objective and subjective data from usability studies to inform design, inform risk minimization, and provide alternative design controls/solutions
- Support the HFE/UE lead in providing preparation for clinical studies and regulatory submissions in accordance with HFE/UE best practices, guidance and standards
- Prepare documentation to support development activities, design controls, DHF, DMR including protocols, task analysis, risk assessment, HFE/UE technical assessments, comparative analysis, HFE/UE reports, data verifications, and regulatory submissions
- Actively communicate with internal and external key stakeholders. Exercising critical thinking & educated HFE/UE judgement to determine appropriate next steps/actions
Skills
- MEDICAL DEVICE/BIOTECH/PHRMA Industries required
- Document writing and validation report exp is required
- End to end human factors experience required from planning to validation and reporting
- Must be able to demonstrate good technical writing skills
- Good communicate skills and experience working with cross functional teams
- Minimum experience needed with medical device but most importantly combination product experience
- Master's degree in Human Factors Engineering, Usability Engineering, or related Psychology and/or Industrial Design domains plus at least 1-2 years' experience working in the regulated medical device and/or biotech industry
- OR Bachelor's degree and at least 2-3 years of Human Factors Engineering/Usability Engineering experience working cross-functionally in the regulated medical device and/or biotech industry
- Master's degree in Human Factors, HFE/Usability Engineering, or other relevant HF/Engineering discipline and 2+ years of industry experience, working in multi-functional, fast-paced corporate environments
- Experience with various HF methodologies such as ethnographic research, interviews, contextual inquiries, focus groups, technical assessments, device UI evaluation, knowledge and comprehension studies, HF professional analysis, task analysis, hazard analysis, risk assessment, formative and summative studies
- Experience working directly with users to gather, synthesize and convert user research into concepts that differentiate products in the market, as well as to develop and evaluate new product features, user interfaces and ergonomic designs
- Experience using low and high-fidelity prototypes to identify and eliminate potential use errors early in the development process
- Experience working in development organizations, particularly virtual development environments contributing to systems design, verification, and validation milestones
- Ability to communicate effectively with mechanical, electrical, software, clinical, regulatory, safety, risk, and quality engineering disciplines
- The position requires good oral and written communication and organizational skills, technical problem solving, the ability to work in teams, critical thinking, the ability to adapt to a rapidly changing environment, and desire to contribute to meaningful and innovative products
- Functional knowledge and experience in the practical application of relevant FDA human factors guidance, regulations and standards, including IEC 62366, AAMI HE75, EN 60601, ISO 14971, MDR, and design controls
Benefits
- Location: Fully remote
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