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在 Kenvue，我們意識到日常護理的非凡力量。我們以一個多世紀的傳統為基礎，植根於科學，是標誌性品牌的品牌 - 包括您已經熟悉和喜愛的 NEUTRGENA®、AVEENO、TYLENOL®®、LISTERINE®、JOHNSON'S® 和 BAND-AID®。科學是我們的熱情所在;關心就是我們的才能。

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我們的全球團隊由 ~ 22,000 名才華橫溢的員工組成，他們的職場文化中，每個聲音都很重要，每一個貢獻都受到讚賞。 我們熱衷於洞察， 創新並致力於為我們的客戶提供最好的產品。憑藉專業知識和同理心，成為 Kenvuer 意味著每天有能力影響數百萬人。我們以人為本，熱切關懷，以科學贏得信任，以勇氣解決——有絕佳的機會等著您！加入我們，塑造我們和您的未來。有關更多資訊，請按兩下 here.

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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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