Sr Analyst , Quality Systems
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- Job ID:
- 2507034180W
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What we do
At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent.
Who We Are
Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. For more information, click here.
Role reports to:
SUP REG QALocation:
Latin America, Brazil, Sao Paulo, Sao Jose dos CamposWork Location:
HybridWhat you will do
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
If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.