- Global Pharmaceutical Manufacturing Orgn.
- Contract Opportunity - Start ASAP
- Melbourne Metropolitan Area
About The Company
Operating as a rapidly growing and dynamic global pharmaceutical manufacturing organisation that develops, manufacturers and markets a range of pharmaceutical products. Our client is now seeking a
Document Coordinator to manage quality related documentation for their Quality Systems and Compliance team.
About The Opportunity
Reporting to the Document Manager, key responsibilities include:
- Support document management processes & coordinate internal quality documentation.
- Manage documentation via Veeva Q & ensure all documents from customers are quality checked.
- Ensure documentation with revised changes are recorded & controlled in the Document Management System.
- Troubleshoot workflows & generate relevant reports.
- Utilise LMS (Learning Management Systems) for data entry.
- Actively participate in team meetings.
About You
- Science or relevant tertiary qualifications.
- Pharmaceutical experience within a GMP and Quality environment.
- Sound experience with Electronic Document Management Systems - ie VEEVA Q, Trackwise, LMS & MS Office skills and Sharepoint.
- Excellent interpersonal & organisational skills.
- Sound attention to detail.
- Good written & verbal communication skills.
- Excellent analytical & quantitative skills.
- Good attention to detail with the ability to prioritise.
- Sound written and verbal communication skills.
Culture & Benefits
This is an excellent Contract Opportunity for a Document Coordinator to join a
large Global Pharmaceutical Organisation to further enhance their skills & experience in the documentation management area.
This is a Contract Role requiring immediate start ASAP.
How To Apply
To apply for this role, please forward your CV in MS Word and click on the APPLY button below.
For further details, please contact Sue Campbell on 0417 994 917 or Maria Julienne on 0491 694 371.
NB - Only shortlisted candidates will be contacted.
