This is a newly created role reporting to the Head of Quality; you will be responsible for Regulatory Affairs and Quality Assurance activities for a rapid-growing company in the Complementary Medicines industry.

Your experience working as part of a team within a fast paced and deadline driven environment will see you excel in this role.

You will need highly developed attention to detail and research skills to maintain regulatory compliance of all new products.

Your key responsibilities will include:

- Developing Evidence Packages and Tables for all new products
- Managing Bulk Specifications
- Compiling Shelf-Life Justifications
- Developing and coordinating new product labels to meet all regulatory requirements such as TGO92 & 116
- Reviewing and submitting Listed Medicines on the ARTG
- Maintaining regulatory compliance of all products
- Managing Change Control for new products
- Managing all Product Stability activities

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📌 Regulatory Affairs Associate (Sydney)
🏢 CMG Holdings Group
📍 Sydney