Company Description
Ferronova is a pioneering biotechnology company combining patented iron magnetic nanoparticle technology and magnetic probe technology "to ensure everyone with cancer receives the surgery and therapy they need, no more, no less". Established in 2016, Ferronova collaborates with leading institutions, including UniSA Future Industries Institute, the University of Sydney, and the University of New South Wales, and has received backing from notable investors, such as Renew Pharmaceuticals (ultragreen.ai), Uniseed and Artesian Ventures, along with grant support from the South Australian and Australian governments. The Company is clinical trial stage, having enrolled 92 patients in multiple trials, and is progressing towards commercialisation in the near to medium term.
Role Description
This is a full-time on-site role for a Chemical Process Engineer based in Adelaide, SA, working as part of a collaborative team including R&D and Production. The role involves designing and managing chemical and process systems using experimentation combined with computer modelling software, controlling and optimizing production processes, performing in-depth analysis, troubleshooting, and ensuring compliance with regulatory, health, safety, and environmental standards. Your effort will directly contribute to Ferronova progressing to late stage clinical trials and commercialisation.
We are looking for an outstanding individual, with a minimum of 5 years' experience in manufacturing and process development in a pharmaceutical environment.
Qualifications
* Master's (or Bachelor's with extensive industry experience) in an appropriate field – Chemical Engineering, Mechanical Engineering or similar
* Knowledge of ISO13485, PICS, FDA QSR, cGMP and associated regulations and documentation
* Proficient in modelling and simulation software such as VisiMix or MixIT, Aspen Plus/HYSYS or equivalent
* A proactive approach to innovation and problem-solving
* Excellent Analytical Skills to diagnose and solve technical challenges
* In-depth knowledge of relevant safety standards and regulations
* Ability to work independently, with good organisation and time management skills to ensure timely delivery of activities
* Strong communication and collaboration skills for effective teamwork
* Experience in medical device or pharmaceutical industry is advantageous
* Proficient with MS Office suite, Google suite and ChemWatch
Close date is 31 March 2026
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