Address
Form of work
SalaryBBBH34459_1708302661 Posted: 19/02/2024
- Eastern Suburbs Sydney, New South Wales
- Permanent
Reporting into the GCP Quality Manager this will be working on site.
ROLE/DESCRIPTION
- All Quality activities relating to GCP and the ongoing clinical trials with sponsor companies.
- Working closely with other departments of the company directing and collaborating with them
- Investigate non-conformance issues
- Working with clinical staff
- Host or co-host Audits
- Line management to one currently, will change over time
- Training of compliance
- Documentation / reporting
- Driving the execution of all things clinical compliance
- Working with senior management on some strategic direction
- Life sciences degree
- Strong knowledge and understanding of GCP
- excellent spoken and written English
- Have worked in a Clinical Quality role previously in Australia or overseas
- Eligibility to work in Australia already
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 Executive 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.
KEY WORDS
Quality Associate, GCP, Quality Assurance Associate, Senior QA Associate, Senior Quality Systems Associate, Quality Assurance Manager, Quality, MAA, CTA, Labelling, Regulatory Operations, Submissions/Documentation, QMS, CAPA, ISO 13485.
