About the company
Work within a large global Biotechnology company that boasts a good company culture that is always expanding.

About the opportunity
The Quality Documentation Coordinator will be responsible for the preparation of protocols and reports and data analysis and will report to the Stability Manager.

Duties

• Preparation of protocols and reports for stability studies
• Data Analysis
• Stability studies will include collecting samples and writing protocols and reports

Skills and Experience

• Bachelor’s degree in science
• Experience in reporting in the pharmaceutical industry
• Strong skills in Word, Excel, PowerPoint and statistics
• Demonstrated experience in a regulated industry with a focus on Stability/QA
• Previous experience within the pharmaceutical industry in a GMP environment
• Excellent time management and organisational skills
• Strong attention to detail
• Be a strong team player

Culture
Although a large, global company, they are able to provide a family-like culture and prides itself in improving the lives of others.

Why this opportunity is right for you
There are two Full-time 6 month contract opportunities available based in the Northern suburbs of Melbourne.

How to Apply
Click apply or contact Jo Turner, Senior Specialist Manager on 03 9938 7100 for a confidential discussion.