
QA Associate
3 days ago
Global Pharmaceutical Organisation
- Global Document Management Systems
- Hybrid Role - WFH & Office Based Opportunity
**About the Organisation**
Operating as a global pharmaceutical manufacturing organisation with world class manufacturing facilities, our client is known for its innovation, premium quality products and strong brand reputation.
- Due to continual expansion, an opportunity has now arisen for a
- **QA Associate with documentation management experience to support global QMS systems & act as a Document Coordinator and control a range of R&D documents.**
**About the Opportunity**
Reporting to the Senior Manager, key responsibilities include:
- Review & route documents for GxP approval & maintain the Document Management System (DMS) database.
- Review documents in terms of compliance with pre-determined template standards & style requirement
- Provide Subject Matter Expertise (SME) advice & assessments on procedural document management systems.
- Facilitate document change control & maintain procedural document templates within the R&D group.
- Ensure compliance of R&D Documentation with current QMS Procedures.
- Effectively liaise with local & global key stakeholders.
**About You**
- Tertiary qualifications in Science, Business or related discipline.
- Sound experience in document management system within a GxP environment.
- Sound document control skills.
- Solid organisation & analytical skills.
- Sound communication & interpersonal skills.
- Sound working knowledge of MS Office Suits of products.
- Ability to work independently & within a team.
**Culture & Opportunities**
This is an excellent opportunity for a
- **Quality Assurance Associate with document management skills to **join a Leading Global Pharmaceutical org. to further develop their skills & experience in document control & management.
- This is a Hybrid Position - WFH & Office based role.**How To Apply**
- For confidential discussion, please contact Sue Campbell on 0417 994 917 or Maria Julienne on 0491 694 371.
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