The position is a full-time role located at our Subiaco (6008) office with an immediate start. This opportunity will allow for growth within the company and exposure to many interesting projects and concepts. Recent graduates or those with experience working in a QA/QC environment are strongly encouraged to apply.

The candidate shall have the following characteristics:

  • Experience working with a Quality Management System e.g. ISO, FDA, CE
  • A strong understanding of physics and engineering principles
  • Ability to work on multiple projects in parallel
  • Strong time management skills
  • Highly organised and good attention to detail
  • Strong communication skills to facilitate working in a team environment

Candidates with the following desirable characteristics will be considered highly:

  • Work experience in a medical device environment (MDR / MDD)

Main job responsibilities:

  • Maintain Technical Files to Regulatory requirements
  • Conduct Post Market Clinical Follow-up studies and associated reports
  • Conduct Post Market Surveillance studies and associated reports
  • Conduct Clinical Evaluation Reports on Medical devices.
  • Conduct medical device shelf-life studies.

How to apply

Remuneration packages consistent with experience will be offered. Please email cover letter addressing the above criteria and CV to This email address is being protected from spambots. You need JavaScript enabled to view it.