R&D Coordinator Self Care - Reckitt Comercial
We are Reckitt
Research & Development
We do the right thing, always, by ensuring we act with responsibility and integrity, by complying with regulatory legislation across the globe, whilst ensuring our products are safe for our consumers and are to the highest quality.
The size of our organisation means you'll have the opportunity to learn and work in different functions within R&D, giving you 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 great organisation.
About 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.
Your 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.
The experience we're looking for
- 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.
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