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R&D Coordinator Self Care - Reckitt Comercial

Reckitt

São Paulo

Híbrido

BRL 80.000 - 120.000

Tempo integral

Hoje
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Resumo da oferta

A global hygiene and health company is seeking an R&D Coordinator to manage regulatory documents for self-care brands in Brazil. This role includes preparing regulatory filings, collaborating with the Global R&D team, and supporting product launches. Ideal candidates hold a degree in Pharmaceutical Sciences and possess strong regulatory knowledge and organizational skills. This is a hybrid role based in São Paulo.

Serviços

Parental benefits
Employee Assistance Program
Life insurance

Qualificações

  • Bachelor's or Master's degree required.
  • Proven experience in regulatory dossier preparation.
  • Familiarity with ANVISA regulations is a plus.

Responsabilidades

  • Prepare regulatory dossiers for submission for Brazil and other LATAM markets.
  • Collaborate with Global R&D team to ensure compliance and timely product launches.

Conhecimentos

Regulatory dossier preparation
Stability protocols
Organizational skills
Communication skills
Cross-functional teamwork

Formação académica

Bachelor’s or Master’s degree in Pharmaceutical Sciences, Chemistry, or related field
Descrição da oferta de emprego
Overview

We are Reckitt, home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. We are a global team united by this purpose. Join us in our fight to make access to the highest quality hygiene, wellness, and nourishment a right and not a privilege. Research & Development is home to highly skilled talents that include Scientists, Engineers, Medical, Clinical and Regulatory professionals, all working to create a cleaner, healthier world. With nine Centres of Excellence, we continually seek out new opportunities by using science, entrepreneurial flair and fearless innovation to develop and enhance our existing portfolio, never compromising on quality or performance.

We do the right thing, always, by acting with responsibility and integrity, complying with regulatory legislation across the globe, and ensuring our products are safe for our consumers and of the highest quality. The size of our organisation means you\'ll have the opportunity to learn and work in different functions within R&D, gaining exposure to different disciplines, teams and environments. You will also have access to our Research and Development Academy, designed to develop our team and allow you to grow in our organisation.

The role

The R&D Coordinator for Self Care brands is responsible for coordinating experimental and administrative activities across assigned projects including New Product Development (NPD), Existing Product Development (EPD), and Business Development Initiatives (BDI). This includes the preparation of technical documentation, regulatory dossiers, and analytical development to support product registration and post-registration processes. The role works in close collaboration with the Global R&D team (UK) and Regulatory Affairs to ensure compliance with current legislation and timely product launches.

Responsibilities
  • Prepare regulatory dossiers for submission for Brazil and other LATAM markets.
  • Prepare documentation related to product registration and post-registration activities.
  • Prepare technical documentation for the submission of new product registrations, in close collaboration with the Global R&D team in UK and Regulatory Affairs teams, ensuring full compliance with current legislation.
  • Provide all necessary technical information to support the successful launch of new products, including formulation details, manufacturing processes, and quality specifications.
  • Collaborate closely with the Global R&D team to ensure technical alignment and secure analytical support, including data packages, method validation, and documentation required for regulatory submissions across LATAM.
  • Design and implement pharmaceutical stability studies in accordance with regulatory guidelines.
  • Develop, validate, and transfer analytical methods, ensuring robustness and reproducibility.
  • Contribute to technical discussions related to dossier content in Trade Associations.
Qualifications
  • Bachelor’s or Master’s degree in Pharmaceutical Sciences, Chemistry, Chemical Engineering, or related field.
  • Availability to work in a hybrid model in our commercial office in Vila Olímpia, SP.
  • Proven experience in regulatory dossier preparation and knowledge of ANVISA regulations.
  • Strong understanding of stability protocols and material characterization techniques.
  • Expertise in CMC Dossiers development.
  • Excellent organizational and communication skills.
  • Experience working in cross-functional and global teams.
  • Familiarity with LATAM regulatory environments is a plus.
  • Advanced English required. Spanish is a plus.
Disclaimer

O Grupo Reckitt não realiza cobranças para a participação em processos seletivos. Caso receba alguma mensagem solicitando pagamento, não responda e entre em contato conosco através das redes sociais ou SAC.
Seguindo a política de direitos humanos, não contratamos menores de 18 anos para essa função.

What we offer

With inclusion at the heart of everything we do, we support our people at every step of their career journey through our Employee Resource Groups. We invest in wellbeing through parental benefits, an Employee Assistance Program, and life insurance for all employees globally. We offer a range of other benefits in line with the local market. Through global share plans we provide opportunities to save and share in Reckitt\'s potential future successes. For eligible roles, we also offer short-term incentives to recognise and reward outstanding results, aligned with Reckitt\'s pay-for-performance philosophy.

Equality

We recognise that great people don\'t always tick all the boxes. We hire for potential as well as experience. All qualified applicants will receive consideration for employment without regard to age, disability, medical condition, colour, ethnicity, race, citizenship and national origin, religion, faith, pregnancy, family status and caring responsibilities, sexual orientation, sex, gender identity, gender expression, and transgender identity, protected veteran status, size, or any other basis protected by applicable law.

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