Senior Scientist – R&D Analytical

Senior Scientist – R&D Analytical

Ce que nous faisons

Chez Kenvue, nous réalisons le pouvoir extraordinaire des soins quotidiens. S'appuyant sur plus d'un siècle d'héritage et enraciné dans la science, nous sommes la maison de marques emblématiques - dont NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON'S® et BAND-AID® que vous connaissez et aimez déjà. La science est notre passion ; Le soin est notre talent.

Qui nous sommes

Notre équipe mondiale est composée de ~ 22 000 personnes brillantes avec une culture d'entreprise où chaque voix compte et chaque contribution est appréciée. Nous sommes passionnés par les idées, l'innovation et l'engagement à fournir les meilleurs produits à nos clients. Avec de l'expertise et de l'empathie, être un Kenvuer signifie avoir le pouvoir d'avoir un impact sur des millions de personnes chaque jour. Nous donnons la priorité aux personnes, nous nous soucions farouchement, nous gagnons la confiance grâce à la science et nous résolvons les problèmes avec courage - et nous vous offrons de brillantes opportunités ! Joignez-vous à nous pour façonner notre avenir et le vôtre. Pour plus d'informations, cliquez sur ici.

Role relève à :

GER TECN PESQ E DESENV

Lieu :

Latin America, Brazil, Sao Paulo, Sao Jose dos Campos

Lieu de travail :

Hybride

Ce que tu vas faire

Kenvue is recruiting a R&D Analytical Senior Scientist based in São José dos Campos, SP, Brazil. This professional will lead strategy and execution of analytical development and accelerated stability studies for innovation projects to attend cosmetic portfolio products at Kenvue, supporting projects from local to global scope. Main responsibilities are planning, execution and evaluation of resources for delivering activities.

This professional will write and review technical documents, including test methods, technical protocols and reports (test method validation, test method transfer and stability studies) following standard operation procedures e quality/regulatory requirements.

Main responsibilities

•Strong sense of urgency is necessary for rapid response to problem solving, troubleshooting and to identify improvement opportunities of current processes.

•Strong sense of independency and autonomy on decision making and clarity/agility on escalating hot topics to leadership levels.

•Clear communication with internal and external stakeholders.

•Capacity to work in a collaborative way with analytical peers and with internal stakeholders.

•Independently manage tasks complexity and communicate data results and main outcomes of the projects, suggesting action plans as needed to support the projects decisions.

•Independently execute laboratory activities, such as test method validations, test method transfers, stability study analysis, analytical investigations and chemical characterization analysis.

•Lead definition of strategy to define protocols of test method validation/transfer and stability studies.

What we are looking for

Required Qualifications:

•A minimum of bachelor’s degree in Chemistry, Chemical Engineering, Pharmacy and/or correlated areas is required

•Experience in pharmaceutical/cosmetic/chemical/food industry is required

•Experience in liquid and gas chromatography is mandatory to that position

•Experience in test method validation/transfer is highly recommended

•Fluent level of English is a must have, as this professional will be exposed to global meetings

Desired Qualifications

•Previous experience in management of stability studies will be considered as a differential.

•Experience in implementing technical projects or in site issues support to manufacturing/production area is a differential.

•Knowledge about the regulations and/or guidelines related to method development & validation for drug products, drug substance and/or cosmetics is desirable for this position.

•It is preferred that this candidate have strong technical writing skills and project management skills.

•Experience in systems as EMPOWER and LIMS is desirable.

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