Senior Medical Affairs Associate for Established Products

At Johnson & Johnson, we believe health is everything.

Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions 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 https://www.jnj.com

Job Function:
Medical Affairs Group

Job Sub Function:
Medical Affairs – Marketed Products

Job Category:
People Leader

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

Job Description:


* Great Place to Work® Certified – 2025


* Johnson & Johnson named a 2025 Fortune World’s Most Admired Company


* Competitive salary package, flexible work practices, award winning benefits


* Continuous training and development

ABOUT INNOVATIVE MEDICINE

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.

Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

Learn more at https://www.jnj.com/innovative-medicine

THE OPPORTUNITY

We are seeking a highly skilled, effective communicator, and knowledgeable Medical Affairs Associate to join our team.

This role is focused on our established products and combines both medical and regulatory responsibilities.

The ideal candidate will have extensive experience in communicating and working with external and internal stakeholders, scientific knowledge, with ability to work with agility and execute on action plans with diligence, being comfortable to work with strict timelines. 

This is a critical and strategic role.

The successful candidate will make a positive impact on patients and healthcare professionals as well as supporting the business through medical and regulatory leadership activities and expertise.

RESPONSIBILITIES


* Provide expertise and project execution on the medical and regulatory components of established products (EP) -related issues and projects in Australia and New Zealand.  This includes Discontinuations, Delistings and Deregistrations, Dear Doctor Letters, and Divestments (transfers of sponsorship) as well as safety issues.

This person will work with the cross functional (XF) team.


* Orchestrate and lead projects related to safety actions and issues within EP


* Leadership of Dear Doctor letters including drafting, coordinating XF reviews, defining distribution plan, audience and timings.  Also includes  consultation and approvals from  the TGA and Medsafe.   Close collaboration with cross-functional teams to ensure regulatory and medical compliance a...