About the role An experienced Regulatory Affairs professional role within a consulting company in Australia. This role offers the opportunity to work with a diverse portfolio of pharmaceutical and healthcare clients, providing both strategic and operational regulatory support across Australia and New Zealand.

You will play a key role in ensuring regulatory compliance, supporting marketing authorisations, and driving successful product approvals and lifecycle management activities. This position requires strong consulting capability, stakeholder engagement, and the ability to manage multiple client projects in a fast-paced environment.

This role can be based anywhere in Australia.

Key responsibilities

- Manage regulatory submissions and lifecycle maintenance activities across Australia and New Zealand

- Ensure compliance with TGA and Medsafe regulations, industry standards, and internal policies

- Develop and implement regulatory strategies to support product approvals, variations, and market expansions

- Provide expert regulatory advice to clients on new and existing pharmaceutical and healthcare products

- Prepare, review, and coordinate regulatory submission dossiers

- Liaise with regulatory authorities, including the TGA, and manage responses to queries and RFIs

- Collaborate with internal teams, global stakeholders,