At Johnson & Johnson, the largest healthcare company in the world, we come together for one purpose: to transform the history of health in humanity.
Diversity & Inclusion are essential to continue building our history of pioneering and innovation, which has been impacting the health of more than 1 billion patients and consumers every day for more than 130 years.
Regardless of your race, belief, sexual orientation, religion, or any other trait, YOU are welcome in all open positions at the largest healthcare company in the world.
When You Join Johnson & Johnson, Your Move Could Mean Our Next Breakthrough.
At Johnson & Johnson Medical Devices Companies, we are using our breadth, scale, and experience to reimagine the way healthcare is delivered and to help people live longer, healthier lives.
In a radically changing environment, we are making connections across science and technology to combine our own expertise in surgery, orthopedics, and interventional solutions with the big ideas of others to design and deliver doctor and patient-centric products and solutions.
We are in this for life.
We are changing the trajectory of human health, YOU CAN TOO.
- In partnership with the LATAM RA PMO executes registration strategies for designated regional projects related to new/existing products, according to local regulation, approved licenses, and RA Hub/Country alignment;
- Adheres to environmental policy and procedures and supports department environmental objectives;
- Works with LATAM RA Leadership and RA Country Owners to ensure rapid and timely approval of new and existing products;
- Assists with ensuring compliance with regulatory agency regulations and interpretations.
- Assists with the preparation of responses to regulatory agencies questions and other correspondence;
- Assists with preparing necessary outlines, summaries, status reports, memos, graphs, charts, tables, and slides;
- Provides solutions to a variety of problems of limited scope and complexity.
- Conducts searches of existing files for requested information;
- Submission of payments/PO in SAP System related to the Regulatory area in LATAM;
- Support to update LATAM database;
- Support to request documents/deliverables in the Request Management System for LATAM;
- Support to download documents from Agile to set up technical dossier in LATAM;
- Support to create the information of products to deliver to ours consults and distributors;
- Partners with other functions to define and obtain regulatory deliverables to assist with local submissions or designated regional projects;
- Updates relevant global, regional and local databases to ensure compliance;
- Maintains and archives all regulatory documentation.
**Qualificações**
**Requirements**:
- Bachelor's degree in health-related courses with a minimum of 1 year of Regulatory experience in a regulated industry (could include pharmaceutical, medical device, or associated consumer industries)
- Fluent in Portuguese and advanced in English (written and verbal)
- Intermediate Spanish level as a plus
- Result-oriented, initiative, proactive
- Team player
- Good communication skills (collaborative approach), open-minded
- Demonstrated ability to handle multiple projects
**Local Principal**
Brasil-São Paulo-São Paulo
- **Organização**
Abbott Prod Oticos Ltda (7602)
**Cargo**
Assuntos reguladores
**Requisition ID**
2206067084W