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Special projects regulatory affairs lead, anz

Jnjmedtech
Posted: 10 June
Offer description

Special Projects Regulatory Affairs Lead, ANZ

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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 https://www.jnj.com

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

Working closely with the APAC RA Regional Lead, and Global PMOs, the Regulatory Affairs Lead will head up the Special Projects team in ANZ and drive the execution of RA initiatives for our medical device business units. Leading by example to the team, you will work collaboratively and partner with key stakeholders and business unit leaders within the organisation and play a pivotal part in ensuring regulatory excellence and compliance for Johnson & Johnson’s suite of cutting-edge medical devices.

Responsibilities


* Leading and developing regulatory strategies for all Special Projects, aligning with internal partners across the organisation (including global PMOs, local RA, Supply Chain, Marketing and Quality etc.), ensuring stakeholders' voices are evaluated within strategies
* Providing prioritisation, capacity management, and efficiency gain options for Special Project Programs in ANZ
* Working collaboratively with country or local franchise RA leaders, leading executions of all Special Projects, and setting up project plans with detailed tasks and timelines to avoid registration misses
* Being accountable for completing Special Project impact assessments, and all RA actions accurately, and ensuring timely MDRiM updates for each RA action, SEP dates, license updates and code linkage to country licenses as per SOPs
* Being part of the APAC RA leadership team and representing ANZ; sharing best practices on Special Project executions, and responsible for achieving and maintaining appropriate metrics for ANZ Programs as per 2025 G&Os
* Adhering to all policies and legislations, and maintaining the highest levels of professionalism, ethics and compliance always
* Recruiting and hiring RA resources as needed, diligently participating in compliance program-related activities, and effectively leading, coaching, and developing a high performing, collaborative team

About You

* Degree and/or post-graduate qualification in Regulatory Affairs, Engineering, Science or related discipline, with minimum 8 years Regulatory Affairs specialist industry experience, with at least 2-3 years in a lead capacity within the medical device industry
* Previous experience managing, or leading projects, with highly developed engagement, negotiation, influencing, and leadership skills
* Experience with regulatory submissions, change and risk management processes, along with strong attention to detail
* Commercial acumen, who is results and solutions focussed, along with excellent communication, prioritisation and time management skills
* Ability to work well under pressure to meet deadlines and to make sound decisions daily concerning regulatory affairs

Why Choose Us

* Competitive remuneration package
* Continuous training and support
* Award-winning leadership development programs
* Inclusive, flexible, and accessible working arrangements
* Equal opportunity employer supporting diversity and inclusion

Our Benefits

* Up to 18 weeks of parental leave to support new parents
* 4 days of volunteer leave to give back to the community
* Option to purchase up to 2 weeks of additional annual leave for extra time off
* Enjoy a dedicated Wellbeing Day to prioritise self-care
* Global Wellness Reimbursement of $780 per year for healthy eating, exercise, or mindfulness activities
* Access to an Employee Assistance Program for personal and professional support
* Enhanced leave provisions for compassionate (caregiver) leave, providing up to 30 days of additional support
* Life insurance coverage for added peace of mind

And much more...

Great Place to Work Certified – 2024

Great Place to Work Certification recognises employers who create outstanding employee experience. The certification process is recognised worldwide as the global benchmark for identifying outstanding workplaces.

Johnson & Johnson – Australia and New Zealand were certified as a Great Place to Work in ANZ in its first year of participation.

All applicants MUST have rights to work in Australia.


Seniority level

* Seniority level

Not Applicable


Employment type

* Employment type

Full-time


Job function

* Job function

Legal
* Industries

Hospitals and Health Care

Referrals increase your chances of interviewing at Johnson & Johnson MedTech by 2x


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