Sr. Analyst, Quality Systems & Compliance (Projects) - Prazo Determinado

Sr. Analyst, Quality Systems & Compliance (Projects) - Prazo Determinado

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 :

GER QA

Lieu :

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

Lieu de travail :

Hybride

Ce que tu vas faire

Kenvue is currently recruiting for:

Sr. Analyst, Quality Systems & Compliance (Projects) - (Prazo Determinado – 9 meses)

Job Description General Header Statement

This position reports into Quality structure based at Kenvue SJC, BRAZIL site.

Who We Are

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. Our global team is made by 22,000 diverse and brilliant people, passionate about insights, innovation and committed to deliver the best products to our customers. With expertise and empathy, being a Kenvuer means to have the power to impact life of 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.

What You Will Do 

The Quality analyst will be responsible for executing quality plans across the region in order to achieve projects of the company related to Quality Management system update to new company strategy including system updates, performance metrics, supplier management, quality management system adequacy, product label & codes change, specification, documentation updates including change contro.l

Key Responsibilities

• Participation on quality projects related to regional and global strategic initiatives
• Build collaboration across different functional areas with business partners
• Deliver the Final Project Objectives
• Develop and Execute Project plans through collaboration with cross functional team members
• Collaborate with quality functions to  meet project deliverables following quality requirements.
• Execite Change control GxP related activities on-time and in compliance with Kenvue procedures and country-specific quality/regulatory requirements
• Identify  risks effectively and assist in identification and implementation of mitigation plans.

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 regulated environment
• Experience in Quality systems,  supplier management, labeling, GxP documentation (SOPs and specifications approval,  Laboratory systems, Change control management) audits/regulatory inspections
• Proven experience in working on virtual teams within dynamic settings in a regional /cross-functional environment.  Ideally 2-3 years.     
• Solid technical (quality/regulatory) knowledge
• Understanding of LATAM GxP regulations  applicable for cosmetics, devices, pharmaceutical  industries.

Desired Qualifications /Technical competences

• Ability to work on cross-functional/regional 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
• Advanced English  
• Advanced Spanish

What’s In It For You

• Competitive Benefit Package
• Paid Company Holidays, Paid Vacation, Volunteer Time, Summer Fridays & More!
• Learning & Development Opportunities
• Employee Resource Groups 
• This list could vary based on location/region

Kenvue is proud to be an Equal Opportunity Employer.  All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

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