Description
Join GSK as a Human Factors Engineer and help design easy-to-use and safe healthcare solutions.
You will work closely with cross-functional teams to understand user needs and bring these insights into the design process.
Responsibilities:
- Lead human-centred design activities throughout all stages of device development to ensure products meet user needs.
- Plan and execute user studies to gather meaningful feedback.
- Conduct user-related risk assessments and integrate findings into design decisions to improve safety and usability.
- Work closely with engineers, regulatory, clinical, and quality teams to solve design and regulatory challenges.
- Manage relationships and communications with external vendors and internal stakeholders to support project goals.
- Contribute to regulatory documentation by preparing clear, accurate sections related to human factors and usability.
Basic Qualifications:
- Degree in Mechanical Engineering, Biomedical Engineering, Human Factors, or a related field.
- Proven experience applying human factors engineering principles in medical device or combination product development.
- Understanding of human factors regulatory guidelines such as IEC 62366 and FDA usability requirements.
- Experience planning and conducting human factors studies.
- Strong communication skills to work effectively within cross-functional teams and with external partners.
Preferred Qualifications:
- Experience with global regulatory submissions and authoring sections of human factors files.
- Ability to analyse user data and translate insights into clear design improvements.
- Familiarity with design for manufacture principles.
- Strong organisational skills with the ability to manage multiple projects and deadlines.
- Evidence of being a proactive team player who adapts well to changing priorities.
- High attention to detail and commitment to quality.
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