Ausbiotech | Medical Devices Regulatory Affairs Associate | south australia
vor 20 Stunden
In this role you will have the opportunity to work on many different medical devices technologies, supporting a wide range of quality and regulatory activities.
Your primary objective is to maximise client commercial success by ensuring appropriate licensing and regulatory compliance of client's products.
In this role, you must be able to advise, support and manage multiple quality and regulatory projects in parallel, liaising with clients, peers and third party subject matter experts.
Your Profile You have formal qualifications in science, engineering with 3 to 5 years' experience working in medical devices regulatory affairs either in industry or a consulting setting.
Exposure to the full product lifecycle is a plus.You have hands-on experience in the preparation of regulatory and technical submissions preferably with the TGA and a strong track record of success.You have a can-do attitude, are a natural problem-solver, a team player with strong focus on results.
You have good attention to detail and at the same time, can keep a focus on the big picture and goals.
You can prioritise and manage several projects at once.You have strong interpersonal skills and enjoy collaborating with colleagues and external stakeholders.
We offer By joining the PharmaLex Australia team you will become part of a team globally renowned as specialists in our field.
Sharing knowledge and expertise with others is part of every day.
We offer a range of flexible working options including part time, varying start and finish times and hybrid office/home working.
We are a diverse workplace and we aim to create a work environment where all can thrive.Our head office is based in St Leonards, Sydney and whilst Sydney is our preferred candidate location we are open to considering candidates based in Brisbane, Adelaide, Canberra or Melbourne.
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