About the chance

At Lead Group, we’re connecting with companies across the MedTech and Pharmaceutical sectors to understand their quality and regulatory recruitment needs.

We’re looking to speak with Quality Assurance and Regulatory Affairs professionals who are considering their next move or would like to hear about relevant prospects as they arise.

Australia-wide expressions of interest — welcoming QA and RA specialists across all states and territories.

Who we’re looking for

We welcome applications from:
Quality Assurance Specialists and Managers
Regulatory Affairs Specialists and Managers
Combined QA/RA professionals
Quality Engineers and Validation Specialists
Heads of Quality and Regulatory Affairs

Your background

You may bring experience in medical devices, pharmaceuticals or biotechnology,



with expertise in one or more of the following:
Quality management systems, ISO 13485 or GM[P
TGA submissions, product registrations and regulatory compliance
EU MDR/IVDR or FDA requirements
Audits, CAPA, complaints and change control
Post-market surveillance and risk management
Design quality, validation or manufacturing compliance

Let’s connect

We’d like to understand your experience, career goals and preferred working arrangements so we can approach you about suitable opportunities.

This advertisement is an expression of interest for current and future opportunities. Your profile will only be shared with a prospective employer with your consent.

📌 Quality Assurance & Regulatory Affairs Specialist Medtech & Pharma Sydney
🏢 Lead Group
📍 Sydney