Prepares and manages regulatory submissions to health authorities.
Ensures products meet local and international compliance standards.

• - Compile and submit regulatory documentation (e.g., to FDA, EMA, TGA)
• - Interpret and apply regulations to product development
• - Maintain licenses and update regulatory filings
• - Liaise with internal teams and external agencies

To apply for this position, click the Apply button below.

Important: Before applying, please compile all the necessary documents — including your CV, certifications, and any other legally required documents — into a single file for upload.

We appreciate your interest in joining our team and look forward to learning more about you!