Sr Analyst , Quality Systems

我们做什么

在 Kenvue，我们意识到日常护理的非凡力量。我们以一个多世纪的传统为基础，植根于科学，是标志性品牌的品牌 - 包括您已经熟悉和喜爱的 NEUTRGENA®、AVEENO、TYLENOL®®、LISTERINE®、JOHNSON'S® 和 BAND-AID®。科学是我们的热情所在;关心就是我们的才能。

我们是谁

我们的全球团队由 ~ 22,000 名才华横溢的员工组成，他们的职场文化中，每个声音都很重要，每一个贡献都受到赞赏。 我们热衷于洞察， 创新并致力于为我们的客户提供最好的产品。凭借专业知识和同理心，成为 Kenvuer 意味着每天有能力影响数百万人。我们以人为本，热切关怀，以科学赢得信任，以勇气解决——有绝佳的机会等着您！加入我们，塑造我们和您的未来。有关更多信息，请单击 here.

Role reports to：

SUP REG QA

位置：

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

工作地点：

混合

你会做什么

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

如果您是残障人士，请查看我们的 残障人士援助页面了解如何申请便利