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Job details

Location
Sydney
Salary
Great salary and benefits package
Job Type
Full Time
Ref
BH-40443-5
Contact
Gemma Staddon
Contact email
Email Gemma
Contact phone
+612 8877 8776
Posted
6 months ago

Job details

Location
Sydney
Salary
Great salary and benefits package
Job Type
Full Time
Ref
BH-40443-5
Contact
Gemma Staddon
Contact email
Email Gemma
Contact phone
+612 8877 8776
Posted
6 months ago
Benefits
• Work with a leading Healthcare company with a global presence
• Collaborative environment with a supportive team in place
• Competitive salary package + bonus

About the Company
Our client is a leading medical devices company in Australia with a global presence focusing on life-changing technologies with leading products across Medical Devices.

About the Opportunity
As a Senior Regulatory Operations Specialist, you will manage regulatory compliance for a diverse range of medical devices as well as championing regulatory operations for the team. Reporting to key stakeholders, you'll play a crucial role in ensuring our client's products meet regulatory standards, impacting the company's market presence positively. This role would suit a self-starter, someone who has experience working in Regulatory Affairs within medical devices, has a strong attention to detail and ability to build strong relationships cross functionally.

Duties
• Monitor and update the regulatory landscape, gathering intelligence, and maintaining the database.
• Collaborate with Regulatory Affairs Specialists to review and approve advertising and promotional materials.
• Support product releases by assisting in the preparation and submission of Product Release Authorization documentation.
• Ensure post-approval commitments to regulatory authorities are planned, tracked, and delivered on schedule..
• Participate in various projects and improvement process, including CAPA projects.
• Represent Regulatory operations in cross-functional interactions with other departments such as Supply Chain, Customer Support, Quality, and IT.
• Collaborate with cross-functional teams to integrate and meet regulatory requirements within Quality Systems.
• Participate in internal and external audits, providing regulatory expertise and follow-up support.
• Engage in interactions with regulatory agencies on defined matters

Skills and Experience
• 3 years' experience in Regulatory Affairs with working knowledge of TGA and medical devices
• Degree qualification in sciences to related discipline
• Strong multitasking and detail orientation
• Strong communication skills
• Proactive and able to work in a fast passed environment
• Strong attention to detail

Culture
Our client fosters an inclusive and collaborative culture, where every team member's voice is valued. Teamwork is at the heart of their success.

How to Apply
Click to apply or contact Gemma Staddon (gstaddon@hpgconnect.com) or Erin Cox (ecox@hpgconnect.com) for a confidential discussion.

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