Kellen Lowrie

Research And Development Test Engineer at Medical Developments International (MDI)

Kellen Lowrie is a Research and Development Test Engineer at Medical Developments International since July 2021. Previously, Kellen served as Examinations Coordinator at the Royal Australian and New Zealand College of Obstetricians and Gynaecologists from January 2018 to January 2020, where responsibilities included coordinating high-stakes medical examinations for over 350 candidates. Kellen also worked as a researcher at the University of Melbourne from November 2016 to November 2017, focusing on nanoparticle-cell interaction analysis. Earlier experience includes a role as an Undergraduate Researcher at Lehigh University, during which Kellen designed a microfluidic chamber to study bacterial biofilms. Kellen holds a Masters Degree with Distinction in Biomedical/Medical Engineering from the University of Melbourne and a Bachelors Degree in Bioengineering and Biomedical Engineering from Lehigh University.

Location

Melbourne, Australia

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Medical Developments International (MDI)

"Delivering emergency medical solutions dedicated to improving patient outcomes"​ Medical Developments International (MDI) is one of Australia’s leading specialised healthcare companies. With an industry leading range of products in the areas of pain management, asthma and resuscitation, plus veterinary equipment, MDI has supplied healthcare professionals and patients innovative solutions since 1971. MDI is a publicly listed company on the Australian Stock Exchange (ASX) with both its head office and state of the art manufacturing facilities located in Victoria, Australia. MDI manufacture the innovative pain relief product, Penthrox® that has been widely adopted by organisations throughout Australia. MDI has a proud history in human and veterinary medicine, throughout Australia as well as internationally. For over 30 years MDI's key products have helped healthcare professionals achieve better health outcomes for their patients MDI is compliant with Good Manufacturing Practices as well as ISO 13485 for the manufacture of several of its products (including both pharmaceutical and medical products). Several MDI products are also CE marked, enabling them to be sold into the European Community.


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51-200

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