Kenvueは現在、以下求人を募集しております。
Sr Analyst , Quality Systems私たちがしていること
私たちKenvueは、日々のケアが持つ驚くべき力を信じています。100年以上の伝統と科学に根ざし、Neutrogena®, Aveeno®, Tylenol®, Listerine®, Johnson’s® and BAND-AID®など、皆様が既にご存じでご愛用いただいているアイコニックなブランドを提供しています。科学は私たちの情熱であり、ケアは私たちの才能です。
Who We Are
私たちのグローバルチームは、インサイトとイノベーションに情熱を注ぎ、最高の製品をお客様にお届けすることに全力を注ぐ、多様で優秀な22,000人以上の社員で構成されています。専門知識と共感力を備えたKenvuerであることは、毎日何百万人もの人々の生活に影響を与える力を持つことを意味します。私たちは、人を第一に考え、全身全霊をもってケアし、サイエンスで信頼を獲得し、勇気をもって解決します。私たちとあなた自身の未来を、共に切り開いていきましょう。
Role reports to:
SUP REG QA場所:
Latin America, Brazil, Sao Paulo, Sao Jose dos Campos勤務地:
ハイブリッドあなたがすること
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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