High growth and rapidly expanding Australian business
- Broad and varied role
- Flexible working conditions
- Exciting opportunity for a Regulatory Affairs professional to join this leading ASX listed Medicinal Cannabis company.
- Newly created role
- Hybrid work on offer
Reporting to the Head of Research and Development this broad regulatory role will see you involved in all aspects of this rapidly growing and expanding business as you take new products to market and develop and execute the regulatory strategy.
Specifically your role will include the followingDevelop, execute and maintain regulatory processes and strategies for product submissionsContribute to product launch teams to ensure timely product introduction.Compile data and documentation to ensure compliant dossiers.Identify deficiencies in product dossiers and implement strategy.Maintain and enhance product dossiersIdentify potential vendors and agencies ensuring compliance.Liaise with external agencies, suppliers or others to ensure timely, compliant submission dossiersMaintain adequate records and documentation of all regulatory mattersMaintain appropriate regulatory licensesParticipate in the GMP vendor qualification processesMaintain necessary systems and proceduresEnsure compliance of promotional material, packaging and labelling legislationsCoordinate and / or conduct audits of documentation or suppliersSupport Quality Assurance as requiredTo be successful in this role you will need the following skills and attributesRegulatory Affiars experience gained in Prescription or OTC environmentsDemonstrated experience working in a GMP manufacturing environmentExperience with FDA submissions highly regardedAppropriate tertiary qualificationsWell developed project management skills