Benefits

• Hybrid working (3 days onsite / 2 days WFH) with flexible office days
• Early Friday finishes + additional wellbeing days off 
• Annual bonus + salary continuance insurance
• Global organisation with strong career development opportunities

About the Company
Our client is a global organisation operating within the animal health sector, supporting veterinary products across multiple international markets. The Australian business works closely with global teams across regulatory, quality and manufacturing to support product registrations and ongoing regulatory compliance. The organisation is known for its collaborative culture and commitment to developing its people, offering employees the opportunity to build long-term careers within a supportive and growing environment.

About the Opportunity
As the Regulatory Affairs Specialist, you will join a small and collaborative regulatory team based in North-West Sydney.

Reporting to the Regulatory Affairs Manager, the role offers exposure across the full regulatory lifecycle, including new product registrations, lifecycle management and labelling activities.

The position supports both the Australian market and international export registrations, working closely with cross-functional teams across development, quality and manufacturing.

With a portfolio focused on companion animal and equine products, the company is continuing to expand its veterinary product portfolio locally as part of a broader global growth strategy, creating opportunities to support new product development and portfolio growth.

If you enjoy taking ownership of your work and being part of a collaborative team where your contributions are valued, this opportunity offers the chance to grow within a globally recognised animal health company.

Duties

• Compile and prepare regulatory dossiers for new product registrations
• Manage lifecycle regulatory activities including variations and label updates
• Review and approve product labelling and artwork for regulatory compliance
• Support new product development projects and product launches
• Liaise with regulatory authorities including APVMA
• Collaborate with cross-functional teams including quality, technical and manufacturing

Skills and Experience

• Experience in Regulatory Affairs, ideally within Animal Health, with exposure to APVMA submissions highly regarded
• Experience preparing or contributing to regulatory dossiers and submissions
• Understanding of regulatory lifecycle management, including variations and label updates
• Strong knowledge of regulatory compliance and labelling requirements
• Candidates from pharmaceutical or other regulated industries will also be considered

Culture
A supportive and collaborative environment that values diversity and continuous development. As part of a close-knit regulatory team, your contributions will have real visibility and impact.
 
How to Apply 
Click apply or contact Jenn Bowder, Senior Recruitment Consultant on 02 8877 8702 for a confidential discussion. 

About Healthcare Professionals Group
Healthcare Professionals Group recruits all positions: executive, permanent, contracting/temp, at all levels, across all areas of healthcare - Pharmaceuticals, Biotechnology, Medical Technology and Clinical Care.

• Medical Affairs & Life Sciences Recruitment - Clinical Research, Market Access, Medical Affairs, Pharmacovigilance, Quality, Data Management, Regulatory Affairs, Scientific;
• Commercial Recruitment - Marketing, Sales, Analytics, Government and External Affairs;
• Business Operations & Infrastructure Recruitment - Administration, Customer Service, Engineering, Finance, Human Resources, IT, L&D, Legal, Manufacturing, Operations, Supply Chain, Warehouse;
• Clinical Care Recruitment - Allied Health, Aged Care, General Practice, Medical Imaging, Medical Management, Medical Specialties, Nursing.