Job Description

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 fast-growing company in the Complementary Medicines industry.

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

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

Your key responsibilities will include: n

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- Developing Evidence Packages and Tables for all current products
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- Managing Bulk Specifications
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- Compiling Shelf-Life Justifications
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- Developing and coordinating new product labels to meet all regulatory requirements such as TGO92 & 116
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- Reviewing and submitting Listed Medicines on the ARTG
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- Maintaining regulatory compliance of all products
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- Managing Change Control for new products
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- Managing all Product Stability activities
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📌 Regulatory Affairs Associate (Sydney)
🏢 CMG Holdings Group
📍 Sydney