engineering
Posted 4 weeks agoEngineer II, Reprocessing Engineering (1 year Fixed Term Contract)
at ResMed
Sydney, AustraliaOn-site
Requirements
- Experience validating cleaning, disinfection or sterilization methods (e.g. bioburden, bacterial reduction determination) Knowledge of communicable pathogens and precautions Working knowledge of global reprocessing standards, process validation methodology and practice
- Experience contributing to technical reports, regulatory documentation, or similar deliverables #LI-APAC Joining us is more than saying “yes” to making the world a healthier place.
Additional details
- Let’s talk about the team As a Reprocessing Engineer II within the Resmed Reprocessing Team, you will be part of a team of subject matter experts responsible for the development and execution of verification and validation of the cleaning, disinfection and labelling of ResMed medical devices.
- The reprocessing team owns, develops and maintains the reprocessing strategy in compliance with relevant regulations; ISO17664-1 and -2, ISO15883, ISO10993, ST98, TIR12, and TIR55.
- The team’s reach extends across various product development groups globally, ensuring that Resmed's products meet healthcare customer expectations through safe and compliant business activities.
- We pride ourselves on constantly adapting and relentlessly improving to maximize the value that we add to the broader organization.
- This is a role for someone who demonstrates solid technical capability and can independently deliver high-quality outcomes while collaborating effectively across teams.
- You will apply sound engineering judgement to solve real-time problems and consistently deliver robust, compliant reprocessing solutions.
- You will create and validate cleaning and disinfection instructions for a wide range of Resmed medical devices, working collaboratively with teams across marketing, medical affairs, product development, and systems engineering.
- You will bring a methodical and detail-oriented approach to ensure scientific rigour is maintained across a variety of complex medical products. Let’s talk
- about the role Develop and optimize reprocessing methods and instructions for the cleaning and disinfection of respiratory medical devices, ensuring solutions are robust and compliant Work collaboratively with cross-functional product development teams including marketing, product development, regulatory, clinical, labelling and quality representatives, proactively identifying risks, trade-offs, and dependencies to influence effective outcomes Manage stakeholder expectations and proactively communicate