Full-time, permanent, work from home 1-3 days per week Values focused culture encouraging accountability, autonomy and collaboration Utilise your engineering and technical experience to make a real difference Are you passionate about improving patient health outcomes? Would you like to join an organisation with an established history where you can work on high-risk critical devices? This role will allow you to tap into your drive, initiative, critical thinking and problem-solving abilities. Reporting to the Team Lead, Post Market Engineering, you will bring your engineering and design control experience to our dynamic and collaborative Post Market Engineering team. This diverse role will be responsible for risk analysis and design activities on our existing endovascular graft implants to meet changing medical device requirements around the globe and take these devices into new markets. Lead and/or assist in post-market design activities for current products including Maintaining Design History Files (DHFs) to ensure continued compliance with current state-of-the-art, Development of information for submissions and responses on current products in existing markets Technical assessment of supplier changes to components and implementation of design changes to enable continued supply of product to market. Testing activities including development of test protocols, liaison with external test facilities, analysis and reporting of test results. Review of product performance and safety, including root cause analysis and design solutions to resolve any identified problems. Manage engineering driven projects or programs. Effective communication of technical analyses and risk assessments to cross-functional stakeholders. Tertiary qualifications in Mechanical Engineering or equivalent essential. Knowledge and experience in the application of Design Control processes essential. Medical devices preferred. Knowledge and experience in the application of Risk Management Techniques essential. Previous experience working within a highly regulated industry. Medical devices preferred. Experience working across multiple projects and disciplines with demonstrated ability to meet deliverables essential. Demonstrated ability to interact effectively and professionally throughout various levels of a Global Organisation. Highly developed technical writing skills and attention for detail. Demonstrated leadership skills with the ability to take ownership. Intermediate statistical data analysis skills and experience essential.