Senior Regulatory Affairs Associate - MedTech, Sydney

At Johnson & Johnson,we believe health is everything.

Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.Learn more at jnj.com .

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world.

We provide an inclusive work environment where each person is considered as an individual.

At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:
Regulatory Affairs Group

Job Sub Function:
Regulatory Affairs

Job Category:
Professional

All Job Posting Locations:
North Ryde, New South Wales, Australia

Job Description:

About MedTech

Fuelled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalised treatments.

Visit us at https://www.jnj.com/medtech to see how your unique talents will help patients on their journey to wellness.

The Opportunity

To support our continued growth, we've created a new opportunity for a Senior Regulatory Affairs Associate in Sydney.

Reporting into the Regulatory Affairs Manager, you will play a key role in ensuring the successful registration, maintenance, and compliance of innovative medical technologies across Australia and New Zealand.

Responsibilities



* Preparing and submitting regulatory applications and documentation to support new product launches, product changes, and ongoing market access across ANZ


* Maintaining regulatory compliance by managing product registrations, responding to regulatory authority requests, and supporting periodic reporting requirements


* Providing regulatory guidance and expertise to cross-functional teams, supporting product development, business initiatives, and audit activities


* Driving continuous improvement by contributing to regulatory best practices, leading process enhancement initiatives, and supporting team capability development


* Building and maintaining effective relationships with regulatory authorities, industry groups, and internal stakeholders to support business objectives and regulatory outcomes

About You



* Degree qualified with minimum 3-5 years demonstrated experience in a regulatory role within medical devices


* Knowledge and understanding of regulatory frameworks and standards including TGA, Medsafe and ISO


* Strong organisation, project management and problem-solving abilities, with strong attention to detail


* Proactive with a consultative approach, and the capacity to engage and work with cross functional teams


* Excellent written and verbal ...