About the company

An established brand and market-leader in health supplements with a broad product range.

About the opportunity

This is a 20-24 week (6 months) assignment working with the Quality Technical team. You will be responsible for Quality Control and Quality documentation to ensure all raw materials, in-process checks, and final product meet the required specifications for distribution.

Duties

• Inspection of incoming goods and documentation against product specification
• Ensure all data is logged and accurately recorded on ERP system
• Batch documentation review and audit
• Sample inspection against finished goods specs
• Generate and review Certificates of Analysis
• Release products for supply in accordance with TGA requirements
• Review and confirm product change control in line with product release
• Liaise with Operational Services to ensure non-conformances are addressed in a timely manner
• Undertake product quality investigations with internal departments and suppliers
• Support Quality Department with continuous improvement initiatives

Skills and Experience

• Degree qualified in science, engineering, or relevant discipline.
• Must have at least 2 years' experience working in GMP environment in Australia.
• Minimum 2 years' experience working in a QC/QA role
• Ideally have experience working in complementary medicines industry
• Ability to work autonomously.
• High level of attention to detail
• Proven problem-solving ability.

How to Apply

Click apply or contact Joanna Murphy, Senior Recruitment Consultant on +61 2 8877 8718 for a confidential discussion.

( SK927795A )