Sr Analyst , Quality Systems

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 :

SUP REG QA

Lieu :

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

Lieu de travail :

Hybride

Ce que tu vas faire

Role overview

The Sr Analyst, Quality Systems will be responsible for delivering quality plans across the region in order to achieve Veeva QMS transf project milestones in several workstreams such as Investigation and CAPA, Change Control, Quality Management System Adequacy, change management, documentation updates including milestones completion reporting, deployments plan coordination and others.

Key Responsibilities

• Take accountability on Latam milestones associated to QMS quality project implementation related to Veeva tech Solution in the region.

• Build collaboration across different functional areas with business partners

• Build alignment with Sponsor, aligns Core and Extended team to deliver the Final Project Objectives

• Develop, manage, and maintain up-to-date Latam project plans through collaboration with cross functional team members

• Ensure seamless coordination across all workstreams, fostering cross-functional collaboration to maintain synchronization and meet project deliverables following quality requirements.

• Provide project implementation activities across all workstreams such as: mapping and scenarios testing, risk management in integration activities.

• Management to track all Latam project smartsheet related activities on-time and in compliance with Kenvue procedures and country-specific quality/regulatory requirements for Veeva Implementation.

• Manage risks effectively, identify potential problems early, and assist in resolving or raising issues as appropriate.

• Effectively prepare and communicate project status updates regarding project milestones, deliverables, and risks within the workstreams and for the broader project

• Support the functional teams as part of the implementation team as Point of Contact and act as the SME for the quality systems’ processes in project scope (i.e: INV/CAPA/Change Control).

What We Are Looking For

Required Qualifications

• Bachelor's degree in pharmacy, chemical engineering or equivalent technical field required

• A minimum of 5 (five) years of relevant professional work experience in the field regulated health industry : Cosmetic/Device/Drug regulations environment

• Experience in Quality systems, investigations and CAPA, Doc Management, GxP records Management, Regulatory Compliance.

• Proven experience in leading virtual within dynamic settings in a regional /cross-functional environment. Ideally 3-5 years.

• Solid technical (quality/regulatory) knowledge

• Understanding of LATAM GxP regulations applicable for cosmetics, devices, pharmaceutical industries.

• Advanced English, Spanish Desirable.

Desired Qualifications /Technical competences

• Ability to lead and motivate teams

• Excellent problem-solving and conflict resolution skills

• Consistent track record to work cross-functionally

• Flexibility and adaptability to thrive in a multifaceted environment

• Attention to detail and a drive for ensuring data accuracy and integrity

• Strong demonstrated collaboration, sense of urgency, analytical, influencing skills

• Must be able to develop and maintain relationships/partnerships and to work collaboratively

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