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Quality Assurance Associate - Pharma - Sydney

i-Pharm Consulting Australia Pty Ltd

Job Description

Job description

Small rapidly growing innovative pharmaceutical organisation holding a niche sector within the life sciences industry.  

Broad based role with lead responsibilities so perfect for a quality professional who wishes a little more responsibility. 

ROLE/DESCRIPTION

 

  • QMS Maintenance
  • Third party management including supplier qualification and risk assessments
  • product testing 
  • Vendor Qualification
  • Supplier audits
  • Investigate non-conformance issues
  • QMS Matrix training 
  • Provide oversight on CA/PA related activities
  • Host Audits
  • Process returns
  • Batch release

 

REQUIREMENTS

  • Life sciences degree 
  • Australian or NZ experience
  • complementary, Rx or generics manufacturing experience 
  • Extensive experience in Quality Controls and/or Quality Assurance
  • ideally packaging or supplies 
  • Experience within a GMP facility is a must
  • ISO 9001
  • Strong continuous improvement acumen

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 Associate, 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.