Job Description
The Documentation Administrator will be responsible for supporting the Document Lead and Project Team to deliver an updated suite of GMP documentation to ensure that the project is successfully delivered on time and on budget. The Documentation Administrator will liase with key project stakeholders to gather and manage information and documents relating to the execution of the project.
Responsibilities will include:
- Document management, updating, reviewing, collating, distributing
- Tracking deliverables and reporting to Document Lead as required
- Working collaboratively within a team
- Positively and proactively supporting the programme with all key stakeholders
Requirements for the role:
- **Preferable** GMP documentation experience and experience working in a highly regulated environment (manufacturing/pharma)
- Outstanding organizational skills and ability to prioritize tasks
- Excellent computer skills, including Microsoft Office and ideally MS Word and Excel
- Exceptional communication and interpersonal skills
- Keen attention to detail and an aptitude for problem solving
- Able to proactively address potential issues
- Collaborative working style and team-player attitude
- Positive and encouraging personality
- Able to learn quickly, be extremely flexible, and able to work autonomously on concurrent projects
- Able to work independently with little supervision
- Highly motivated with a strong work ethic
Able to thrive in a high-volume, deadline-driven work environment
*** This is a six month assignment ***
APPLY NOW or call (03) 9020 1999 for further information
