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.