Regulatory Affairs Associate

Benefits

• Opportunity to work with cutting-edge medical device technologies
• Hybrid working arrangements
• Competitive salary and progression opportunities

About the Company
An innovative medical device company at the forefront of healthcare solutions, dedicated to enhancing the well-being of patients worldwide.

About the Opportunity
Our client is looking for someone to join their dynamic team as a Regulatory Affairs Associate responsible for ensuring regulatory compliance of medical devices in the ANZ region.

Duties

• Prepare regulatory submissions for medical devices in line with local regulations.
• Assist in maintaining regulatory documents, including technical files and design dossiers.
• Interact with regulatory authorities to address inquiries and compliance issues.
• Stay updated on industry trends and regulatory changes.
• Support post-market activities for product compliance.
• Review packaging materials for compliance and registration.

**Please note, the ideal candidate has unrestricted working rights in Australia

Skills and Experience

• Graduate qualifications in science (essential).
• In-depth knowledge of medical device regulatory compliance and 2 years’ experience in regulatory submissions.
• Strong attention to detail.
• Excellent written and verbal communication skills.
• Strong interpersonal skills.

Culture
Our client’s company culture encourages collaboration and autonomy. We work as a united front, review each other's work, and prioritize transparency and trustworthiness. You'll have the opportunity to work on your projects while also being part of a supportive team.

How to Apply
If you're ready to take on this exciting opportunity and meet the qualifications outlined above, click "Apply" or contact Erin Cox ecox@hpgconnect.com or Gemma Staddon gstaddon@hpgconnect.com for a confidential discussion.