Regulatory Affairs Manager - Diagnostics

i-Pharm Consulting
Victoria, Melbourne, Australia
Closing date
22 Sep 2020

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Regulatory Affairs
Full Time
Contract Type
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Regulatory Affairs Manager - Medical Devices and Diagnostics - Melbourne Based


A Regulatory Affairs Melbourne is required for an exciting growing medical devices and diagnostics company building their global operation from Melbourne.

The company has recently had a large capital injection globally providing an exciting phase in their growth.


  • full management of regulatory work with expanding scope of work on a global scale
  • Regulatory Affairs strategy
  • driving the execution of submissions mostly to TGA, Medsafe but also further down the line in ROW & US FDA
  • Manage the document control function
  • Product approval
  • working closely with Marketing, R & D and post market surveillance
  • full exposure to working on market commercial entry
  • work closely with scientists / engineers
  • maintain regulatory registrations
  • working through product recalls
  • Regulatory liaison for international matters relating to product file compliance / labelling


  • Life sciences degree (pharmacy preferred)
  • Experience with TGA & Medsafe
  • Global product submissions experience
  • Regulatory work supporting R&D operations
  • Regulatory Strategy
  • Worked previously supporting manufacturing and R & D previously
  • TGA, Medsafe, ROW, US FDA
  • ISO 9001 / 13485 knowledge
  • Electronic QMS in a medical device setting (ISO 13485)


i-Pharm Consulting is a specialist Recruitment Company servicing the global Pharmaceutical industry. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.


If you would like to discuss this vacancy further, please call Senior Consultant, Tom Desborough on +61 (0) 2 8310 5843, or email If this role is not suitable, Tom is also available to discuss other possible positions or answer any general questions regarding your career and the current market.


Quality Engineer, Quality Manager, Senior QA Associate, Senior Quality Systems Associate, Quality Assurance Manager, Quality, MAA, CTA, Labelling, Regulatory Operations, Submissions/Documentation, QMS, CAPA, ISO 13485.

Principal Consultant, Senior RA Associate, Senior Regulatory Affairs Associate, Regulatory Affairs Associate, Regulatory Affairs Manager, MAA, CTA, Labelling, Regulatory Operations, Submissions/Documentation, Regulatory Training, Regulatory Trainer, Renewals.

Life Sciences recruitment is what we do.

We are an award-winning international life sciences recruitment company with offices in London, New York, Munich, Singapore and Sydney.  In a highly competitive market-place, we connect top talent with the very best opportunities.


Our clients include many of the most successful and innovative Pharmaceutical, Biotechnology, and Medical Devices companies, as well as a range of Contract Research & Manufacturing Organisations, Healthcare Agencies and Consultancies.


With offices across 3 continents, we have teams servicing the major global life science hubs. We combine local knowledge, with a global network of contacts that allows us to bring together talent and opportunity when it matters most.

Contact Us
  • 212 New King’s Road
  • London
  • SW6 4NZ
  • GB
  • +44 (0) 20 3189 2299
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