Regulatory Affairs Specialist

Há 7 dias


Sao Paulo, Brasil Johnson & Johnson Tempo inteiro

Description

Kenvue is currently recruiting for:
**Regulatory Information Management (RIM) Specialist**

This position reports into Manager, Global Reg Strategic Compliance and is based at Brazil. São Paulo Capital.

**Who we are**

At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent. Our global team is made by 22,000 diverse and brilliant people, passionate about insights, innovation and committed to deliver the best products to our customers. With expertise and empathy, being a Kenvuer means to have the power to impact life of millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage - and have brilliant opportunities waiting for you Join us in shaping our future-and yours.

**Role reports to**: Manager, Global Reg Strategic Compliance

**Location**: Brazil - São Paulo Capital.

**What you will do**

Key Responsibilities
- Develop and maintain PowerBI Dashboards and reports for Regulatory systems and databases.
- Analyze and interpret data to identify trends and provide insights.
- Collaborate with cross-functional teams to ensure timely and accurate publishing and compilation of regulatory submissions.
- Provide training and support to colleagues on RIM systems and processes based on current and emerging compliance regulations and processes.
- Stay up-to-date with industry trends and regulatory changes to ensure compliance.
- Continuously improve RIM processes and systems to enhance efficiency and effectiveness.
- Identify departments that may be impacted by changes to government regulations and provide guidance on compliance issues.

Organize information for presentations that provide regulatory agencies with relevant information regarding department practices.

**Qualifications**:
**What we are looking for**

Required Qualifications
- Bachelor's degree in a related field or equivalent experience.
- Extensive Microsoft PowerBI and Power Query experience.
- Excellent communication and interpersonal skills to interact with internal and external team members.
- Strong analytical and problem-solving skills.
- 2-4 years of experience in regulatory information management or a related field.
- Excellent attention to detail and organizational skills.
- Ability to work independently and as part of a team.
- Ability to analyze and interpret complex information and provide guidance to project teams.
- Diligent with strong organizational skills.

Desired Qualifications
- Proficiency with Microsoft Power Automate and Microsoft SharePoint
- Proficiency in RIM systems and databases.
- Understanding of the regulatory publishing and submission process.
- 2-4 years of related experience in regulatory information management (RIM) data analysis.
- Strong understanding of federal and local regulations and their impact on the department.

**What’s in it for you**
- Competitive Benefit Package*
- Paid Company Holidays, Paid Vacation, Volunteer Time, Summer Fridays & More
- Learning & Development Opportunities
- Employee Resource Groups
- This list could vary based on location/region

Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

Primary Location Latin America-Brazil-São Paulo-São Paulo

Job Function Regulatory Affairs



  • Sao Paulo, Brasil Edwards Lifesciences Tempo inteiro

    Make a meaningful difference to patients around the world. From design to production, our Regulatory Affairs teams help guide our innovative technologies through complex international regulatory environments. Working in partnership with external government and regulatory authorities, and alongside diverse internal stakeholders, your close attention to detail...


  • Sao Paulo, Brasil Thermo Fisher Scientific Tempo inteiro

    At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through...


  • Sao Paulo, Brasil Unilever Tempo inteiro

    **Unilever is currently hiring for a Regulatory Affairs Manager based in São Paulo.** **Unilever** is the place where you can bring your purpose to life with the work that you do - creating a better business and a better world. We are looking for talents that would like to join this exciting journey with us. Our **R&D Brazil Beauty & Wellbeing** team is...


  • Sao Paulo, Brasil The BIG Jobsite Tempo inteiro

    Product Steward who have the overall coordination to manage product stewardship reviews (e.G GHS regulations), existing and emerging regulations, labelling and other requirements which comprehends Latin America region. These activities may include the development of safety data sheets and cross functional trainings;Ensure company operatesin conformity with...


  • São Paulo, Brasil Edwards Lifesciences Tempo inteiro

    Make a meaningful difference to patients around the world. From design to production, our Regulatory Affairs teams help guide our innovative technologies through complex international regulatory environments. Working in partnership with external government and regulatory authorities, and alongside diverse internal stakeholders, your close attention to...


  • São Paulo, Brasil Edwards Lifesciences Tempo inteiro

    Make a meaningful difference to patients around the world. From design to production, our Regulatory Affairs teams help guide our innovative technologies through complex international regulatory environments. Working in partnership with external government and regulatory authorities, and alongside diverse internal stakeholders, your close attention to...


  • Sao Paulo, Brasil Edwards Lifesciences Tempo inteiro

    Make a meaningful difference to patients around the world. From design to production, our Regulatory Affairs teams help guide our innovative technologies through complex international regulatory environments. Working in partnership with external government and regulatory authorities, and alongside diverse internal stakeholders, your close attention to detail...


  • Sao Paulo, Brasil Caldic LATAM Tempo inteiro

    **Responsabilidades e atribuições** - Coordinate and request technical information (GMO, Prop 65, Etc.) from suppliers - Create/maintain product specifications for ingredients, resale and manufactured products - Backup for ticket assignment/triage. - Maintenance of Portal documentation/connections - Maintain SpecSafe contacts - Other tasks as...


  • Sao Paulo, Brasil Caldic LATAM Tempo inteiro

    **Responsabilidades e atribuições** - Coordinate and request technical information (GMO, Prop 65, Etc.) from suppliers - Create/maintain product specifications for ingredients, resale and manufactured products - Backup for ticket assignment/triage. - Maintenance of Portal documentation/connections - Maintain SpecSafe contacts - Other tasks as...


  • Sao Paulo, Brasil Parexel Tempo inteiro

    **Skills and knowledge**: Regulatory Affairs Consultant should have solid local expertise in submitting Clinical Trials to Health Authority in Brazil. This role will be responsible for managing and coordinating the regulatory submission strategy for a large number of clinical trials in Brazil. Also, will coordinate and manage flow of information, track...


  • Sao Paulo, Brasil Parexel Tempo inteiro

    timely performance of work within a project scope to the quality expectations of PC and the client. When serving as a Project Lead or Work Stream Lead, a consultant secures the work of the entire team or work stream is delivered on time and that it meets client’s and PC’s quality. **Skills and knowledge**: Regulatory Affairs Consultant should have solid...

  • Regulatory Specialist

    3 semanas atrás


    Sao Paulo, Brasil Ashland Tempo inteiro

    Ashland Inc. Are you the kind of person that is always thinking, sketching, seeking, and adjusting? Who needs to understand how things work and then figure out how they can work better? Are you a passionate, tenacious, solver who loves to work with others who share your drive? Are you positive, constructive, and ingenious? Are you always solving? Then...


  • Sao Paulo, Brasil Stryker Tempo inteiro

    **What We Want** - ** Detail-oriented process improvers**. Critical thinkers who naturally see opportunities to develop and optimize work processes - finding ways to simplify, standardize and automate. - ** Self-directed imitators. **People who take ownership of their work and need no prompting to drive productivity, change, and outcomes. - ** Analytical...


  • Sao Paulo, Brasil Johnson & Johnson Tempo inteiro

    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...


  • São Paulo, São Paulo, Estado de São Paulo, Brasil Tata Consultancy Services Tempo inteiro

    Come to one of the biggest IT Services companies in the world!! Here you can transform your career! Why to join TCS? Here at TCS we believe that people make the difference, that's why we live a culture of unlimited learning full of opportunities for improvement and mutual development. The ideal scenario to expand ideas through the right tools,...


  • Sao Paulo Metropolitan Area, Brasil Tata Consultancy Services Tempo inteiro

    Come to one of the biggest IT Services companies in the world!! Here you can transform your career!Why to join TCS? Here at TCS we believe that people make the difference, that's why we live a culture of unlimited learning full of opportunities for improvement and mutual development. The ideal scenario to expand ideas through the right tools, contributing to...


  • Sao Paulo Metropolitan Area, Brasil Tata Consultancy Services Tempo inteiro

    Come to one of the biggest IT Services companies in the world!! Here you can transform your career!Why to join TCS? Here at TCS we believe that people make the difference, that's why we live a culture of unlimited learning full of opportunities for improvement and mutual development. The ideal scenario to expand ideas through the right tools, contributing to...


  • São Paulo, Brasil Tata Consultancy Services Tempo inteiro

    Come to one of the biggest IT Services companies in the world!! Here you can transform your career!Why to join TCS? Here at TCS we believe that people make the difference, that's why we live a culture of unlimited learning full of opportunities for improvement and mutual development. The ideal scenario to expand ideas through the right tools, contributing to...


  • São Paulo, Brasil Tata Consultancy Services Tempo inteiro

    Come to one of the biggest IT Services companies in the world!! Here you can transform your career!Why to join TCS? Here at TCS we believe that people make the difference, that's why we live a culture of unlimited learning full of opportunities for improvement and mutual development. The ideal scenario to expand ideas through the right tools, contributing to...


  • São Paulo, Brasil Edwards Lifesciences Tempo inteiro

    Make a meaningful difference to patients around the world. From design to production, our Regulatory Affairs teams help guide our innovative technologies through complex international regulatory environments. Working in partnership with external government and regulatory authorities, and alongside diverse internal stakeholders, your close attention to...