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Scientist II - R&D Analytical

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Kenvue recrute actuellement pour un :

Scientist II - 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

This individual will lead the strategy and execution of analytical deliverables on North America Self Care (OTC) projects. This includes defining the analytical strategy, execution planning, timing, resource requirements and interdependencies to complete the project deliverables. The Scientist II, R&D Analytical is responsible for performing chemical analysis, conducting research programs, and developing research proposals to meet exploratory objectives in product discovery:

Key Responsibilities

  • Lead and manage analytical research projects in R&D department focused on launching new products and support the Kenvue´s product pipeline according to FDA and Health Canada Authorities

  • Validate and transfer analytical methods to support product development and life cycle management projects

  • Collaborate with cross-functional teams to drive scientific advancements

  • Provide technical expertise in analytical instrumentation and data analysis

  • Stay current with industry trends and technologies to drive innovation

  • Execute analytical test evaluations and analyses and other projects

  • Communicate clearly with the internal organization and with the global teams in forums related to projects from strategy definition to project execution.

  • Collaborate effectively with project members following priorities, checkpoints and timelines to guarantee project milestones.

  • Write technical documents to support product registration, quality and compliance policies – protocols and reports related to test method validation, transfer and stability studies or other related documents applied to drug products.

  • Support investigations due to analytical validation, transfer and stability studies.

  • Work collaboratively in partnership with analytical areas in the globe to leverage existing studies and knowledge generated in other sites of the organization.

  • Find opportunities to improve processes or project timelines when appropriate.

  • Communicate effectively analytical leadership on issues which require escalation.

What we are looking for

Required Qualifications

  • A minimum of a bachelor’s degree in Chemistry, Chemistry Engineering or Pharmaceutical Chemistry.

  • Solid experience in the pharmaceutical industry in R&D Analytical

  • A strong analytical background in HPLC, UPLC, GC, dissolution and other analytical techniques is required.

  • Experience with method validation and method transfer is required.

  • Experience with stability studies is required.

  • Solid understanding of analytical and physical testing capabilities

  • Strong analytical and problem-solving skills.

  • Experience performing/ evaluating statistical analysis of the analytical studies conducted.

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

  • Excellent verbal and written communication abilities.

  • Advanced level of English is required for this position (oral for active participation in global meetings and written communication).

Desired Qualifications

  • Experience working in Analytical Chemistry supporting new product development and life cycle management projects in a Consumer Health environment

  • Excellent communication and collaboration skills

  • Experience with Empower chromatography data system, using electronic laboratory notebooks (ELN), and LIMS systems.

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

  • Intermediate level of Spanish can be considered a differential.

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