Description
Kenvue is currently recruiting for:
Sr. Analyst, Quality Systems & Compliance (Projects)
Fixed term – 12 months
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.

What You Will Do
The Quality analyst will be responsible for delivering quality plans across the region in order to achieve project separation milestones in several workstreams such as regulatory licensing , inspection readiness,, quality management system adequacy,, product label & codes change management, documentation updates including change control coordination and others.

• Participation on quality projects related to separation program

• 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.

• Change control opening and management to track all Gx P 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.

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, labeling, Gx P documentation (SOPs and specifications approval, 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 Gx P regulations applicable for cosmetics, devices, pharmaceutical industries.

• 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.

Primary Location Latin America-Brazil-São Paulo-São José dos Campos

Job Function Quality Assurance