A distinguished Australian medical device company that manufactures and distributes a vast range of medical devices and surgical products. The company strives to offer innovative solutions to make a difference to patients lives. They have a collaborative culture and pride themselves on their environmentally sustainable practices.
About the opportunity
You will be required to be on-site every day at their Western Sydney office. You will gain regulatory experience by supporting the team to ensure the company portfolio of medical devices are registered and up to date both locally and overseas. You will also liaise with both internal and external stakeholders to support all regulatory aspects of the company and to ensure compliance with relevant guidelines.
Support the team to ensure and track new registrations of medical devices with the ARTG
Management of technical file system and ERP database to ensure listings and documents are accessible, accurate and up to date
Liaise with relevant government bodies and external stakeholders in relation to Regulatory Affairs
Organise the payment of company registration requirements to relevant bodies
Assist with Regulatory response to tender submissions
Assist with internal audit processes
Assist with product recall activities
Keep abreast and advise of regulatory changes and how they impact company product compliance
Review labels and advertising to ensure regulatory compliance
Review manufacturing documents for regulatory compliance
Skills and Experience
A minimum of bachelor's degree in a life sciences related discipline
Experience in Regulatory Affairs
Ability to interpret and write complex technical documents
Ability to communicate government policy changes
How to Apply
Click apply or contact Madeleine Byrnes, Sourcing Consultant on 0288778703 for a confidential discussion.
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