Manager Cross-Regional Regulatory Affairs - Fixed Term (12 months)

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:
São Paulo, Brazil

Job Description:

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 Johnson & Johnson Innovative Medicine

We are searching for the best talent for these 2 positions of Manager Cross-Regional Regulatory Affairs - Fixed Term (12 months), based in São Paulo, Brazil.

Regional Regulatory Strategy Implementation

Drives and leverages cross-regional synergies and efficiencies


* Responsible for the development of strategic implementation plans.


* Understands regional and local requirements and advises the Global Regulatory Team (GRT), Compound Development Team (CDT) and regional teams on implementation issues pertaining to regional regulatory strategies.


* Participates as a member of the project related GRT; supports the GRT in the implementation of regional input into compound development, registration and life cycle management.


* Responsible for the implementation of the regional regulatory strategy, including the regulatory submission plans, in line with R&D, regional and local business objectives.


* Understands how supply chain decisions impact registrations in the regions.


* Develops and updates contingency plans for the execution of regional regulatory strategies and refines regional plans as new data become available


* Leads the Regional Working group to ensure timely execution of product objectives, and aligns regional deliverables with those of the global teams.


* Facilitates tactical implementation at the regional level, and ensures ongoing and effective communications with the regional and global teams on product activities and issues, related to strategic execution.


* Represents the regions and provides input on implica...