Regulatory Affairs Associate
- Sydney
- Salary:Competitive Salary Package + Bonus
- SalaryCompetitive Salary Package + Bonus
- LocationSydney
- Job type Full Time
- DisciplineRegulatory Affairs
- ReferenceBH-40487
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Regulatory Affairs Associate
Job description
Benefits
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
Skills and Experience
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.
- Opportunity to work with cutting-edge medical device technologies
- Hybrid working arrangements
- Competitive salary and progression opportunities
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.
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.
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.