Aps Level 6

3 weeks ago


Canberra, Australia Australian Government - Department of Health Full time

APS Level 6
- $88,439 - $99,772
- Fairbairn, ACT

This ongoing role at the Therapeutic Goods Administration is a great opportunity to contribute to the development of regulatory policy for the manufacture of medicines. You'll be working within a supportive team to provide strategic and operational support in relation to regulatory reforms and business planning.

Working with a high level of autonomy and as part of a team, the successful applicant will contribute to the regulatory reform projects within MQB.

The key responsibilities are to:

- Undertake the planning, implementation and post-implementation review of regulatory reforms (which may include legislative change) and business improvement projects across the Group, Division and Branch. At the current time, the main focus of the role will be on development and implementation of reforms to the regulation products that are supplied as ‘unapproved goods’, including medicinal cannabis and psilocybin.
- Engage with external stakeholders such as Government Departments, therapeutic good sponsors, manufacturers of therapeutic goods, peak bodies, associations, and consumer groups to assist in the successful delivery of projects
- Under limited supervision contribute to planning, coordination and/or conduct of:

- Ministerial briefs, materials for external and internal stakeholder meetings, legislation and regulatory amendments, risk based business planning & reporting.
- Business projects identified in the branch business plan associated with regulation, cultural improvement and people capability.
- Assisting in the identification and implementation of process improvements and providing technical advice to a range of internal and external stakeholders.


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