Description:
Benefits
Develop expertise across quality and validation
Supportive, collaborative team environment
1 Year Fixed Term contract with the potential to extend
About the company
Our client is a global medical technology organisation with a strong local presence and international reach, with a passion for innovation.
About the opportunity
In this 12-month fixed-term role, you’ll support project documentation and validation requirements. You will also partner with Quality, Regulatory, and Engineering teams to manage documentation for a validation, ensure audit readiness, and contribute to the seamless transition of quality records and updates. A strong focus on attention to detail, timelines, and quality frameworks will be essential to success.
Duties
-
Prepare and manage documentation for validation and audit readiness
-
Support Quality and Regulatory teams with documentation updates
-
Collate and manage technical project records and status reports
-
Generate project slides, meeting documents and reports
-
Assist cross-functional teams with document coordination and planning
Skills and Experience
-
Experience in documentation coordination or quality systems
-
Strong communication and time management skills
-
Skilled in Microsoft Office and digital documentation tools
-
Attention to detail and ability to manage deadlines
-
Experience in regulated industries (medical, pharma or healthcare)
-
Familiarity with WHS and quality compliance standards
-
Ability to work across teams and manage competing priorities
Culture
Inclusive, fast-paced, and quality-driven, with a strong commitment to teamwork and professional development.
How to Apply
Click apply or contact Michelle Vermaak on 02 8877 8760 for a confidential discussion.