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James Cassidy
Life Science

+353 1 5079250
[email protected]
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Details

Principal Human Factors Engineer


Reference:JCAO1104 Location: Dublin
Qualification:DegreeExperience:5-7 Years
Job Type:PermanentSalary: Not Disclosed
May be suitable for: Snr R and D Engineer

Our client a global healthcare currently seek a Principal Human Factors Engineer to join their team. The role is party of a global group that are working o development of a portfolio of medical devices.


Role/Responsibility

  • Lead the User Interface development (Human Factors and Usability Engineering) of a new Platform in line with relevant guidelines and standards.
  • Develop Human Factors Strategy as key part of development program to conclude with successful Design Validation
  • Develop User Requirements of device, labelling and packaging elements of the combination product based on detailed understanding of innovator device product and the intended user profile.
  • Drive these User Requirements through the development program, integrating Risk Management considerations throughout the process.
  • Working closely with Design Engineers ensure that Industrial Design is reflective of the User Requirements and iteratively tested throughout the inhaler development program.



Skills/Experience:
  • Scientist or Engineer with considerable experience in the Medical Device or Pharmaceutical Industry, preferably in the development of Respiratory Combination Products.
  • Strong experience in Human-centered design methodologies
  • Experienced in leading the execution of simulated testing from early patient handling studies through to Design Validation / Summative Human Factors studies.
  • Extensive experience of the integration of Risk Management considerations and User Requirements into iterative, patient-centered Device Design.
  • Proficient in Adobe Illustrator graphics tool.
  • Confidence in execution of a development program within the requirements of Design Control, Risk Management (ISO14971), QMS (ISO13485), Human Factors and Usability standards and guidance (incl ISO62366, HE75), EU MDR etc.
  • Excellent verbal and written communication skills including technical reports and regulatory dossier preparation.




For further information please contact James Cassidy [email protected] or call in confidence 086 02043222