QC/QA Associate

About the company/role:

Our client is a fast-growing Australian TGA licensed manufacturer of complementary medicine with a diverse range of products. This role offers a hands on experience in regulatory documentation, product specifications and QMS. You will be part of a supportive, growth focused team, reporting to the Head of Quality.

Focus Split:

• 70% Regulatory documentation and compliance
• 30% QC documentation and production verification

Duties:

• Prepare and maintain raw material, finished product and packaging specifications
• Create and manage regulatory documents, including labels and cartons, to ensure compliance
• Review label/carton/foil proof to ensure it complies with TGA guidelines
• Support the maintenance of the Quality Management System (QMS)
• Prepare and review BMR/BPR (Batch Manufacturing & Packaging Records)
• Check and verify batch documentation for production records accuracy
• Support QA/QC team processes

Skills/experience:

• 2-3 years' experience in regulatory affairs, quality assurance or quality control within pharmaceutical or complementary medicine space
• Familiar with TGA guidelines and regulatory documentation
• Strong attention to detail for accuracy and compliance
• Team player with a positive and flexible attitude
• Must hold PR or Citizenship

Culture & Benefits:

• Work with a supportive QA Manager in a stable, reputable company
• Opportunity to strengthen your regulatory skills and grow within the business
• Be part of a collaborative team environment that values quality and teamwork

Apply

If you think this could be the role for you then please apply now Please send us a cover letterAND a detailed resume in WORD format (PDFs can be corrupted / not processed).

Or, if you have any questions, please contact Priangel on

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