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 opportunities as they arise.

Australia-wide expressions of interest — welcoming QA and RA professionals 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