Regulatory Project Manager - Join rapidly growing Australian HQ R & D operation. This is a leading Australian Biopharmaceutical with globally recruiting a Regulatory Affairs Project Manager for their Australasian HQ office. Their key products are in development & they are looking to take these key offerings through to commercialisation and beyond. This is a fantastic opportunity to expand your regulatory affairs skills within a HQ development environment.
- Australian Biopharma
- Early stage product development
- Opportunity to rapidly expand regulatory skillset
What You Will Gain:
- Broad based experience with International exposure.
- Lucrative Development experience
- Good project management exposure
THE ROLE:
Act as regulatory affairs project lead to assigned projects and ensure products are taken through key stages to registration in 2009/10. Work across the regulatory affairs dossier lifecycle, inc pre clinical and cmc documentation. Will be involved in International submissions including the US and Europe.
Requisite Skills and Experience:
Seasoned regulatory affairs professional with circa 3- 7 years regulatory affairs experience. Ideally International exposure (European) Ideally experience working in a Head Quarter environment. Life Sciences, pharmacy or chemistry degree. Post grad qualification an advantage but not necesssary.
Hays Pharma are an international Search & Selection firm providing resourcing solutions to the pharmaceutical industry. We have a proven track record recruiting within the Regulatory Affairs market & have a dedicated team appointed to this function. Having established relationships with the worlds leading companies in Biotech, Pharmaceutical, Devices, Clinical Research & Consulting we are ideally placed to find our candidates their next permanent or contract position in Regulatory Affairs.
This job was posted 30+ days ago, and has expired.
