Senior Regulatory Affairs Manager - Medical Devices

Employer
i-Pharm Consulting
Location
Australia, New South Wales, Sydney / Victoria, Australia, Melbourne
Salary
Negotiable
Closing date
4 Oct 2019

View more

Discipline
Regulatory Affairs
Hours
Full Time
Contract Type
Permanent
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JOB TITLE

Senior Regulatory Affairs Manager - Medical Devices - Melbourne Based

JOB SUMMARY

A Senior Regulatory Affairs Manager is required for an exciting growing medical devices company. This particular company is under the global spotlight building their global operation from Melbourne.

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

ROLE/DESCRIPTION

  • Broad based Regulatory role
  • Regulatory Submission to ANZ
  • regulatory strategy
  • Line Management to 3
  • Global product registrations
  • CE Marking
  • Regulatory Strategy
  • Working with the key stakeholders in the business

REQUIREMENTS

  • Life sciences degree (pharmacy preferred)
  • Extensive experience in Australian Regulatory Affairs (and New Zealand ideally)
  • Experience with TGA and Medsafe
  • Global product registrations
  • Reimbursement experience
  • Line Management experience
  • People management would be a bonus
  • Electronic QMS in a medical device setting
  • visa / eligiblity to work in Australia

ABOUT i-PHARM CONSULTING

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.

www.i-pharmconsulting.com

TO APPLY

If you would like to discuss this vacancy further, please call Senior Consultant, Tom Desborough on +61 (0) 2 8310 5843, or email tdesborough@i-pharmconsulting.com. 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.

KEY WORDS

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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