Sr. Quality Analyst – Fixed term role 1 year

Sr. Quality Analyst – Fixed term role 1 year

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:

GER GAR QA SR

Location:

Latin America, Argentina, Buenos Aires, Pilar

Work Location:

Hybrid

What you will do

Sr. Quality Analyst – External Manufacturer
Location: Pilar, Argentina

At Kenvue, we’re redefining the future of self-care and wellness. Join us as a Sr. Quality Analyst focused on External Manufacturers (EMs) across LATAM and help ensure our products meet the highest quality standards through strong partnerships, regulatory compliance, and continuous improvement.

What You’ll Do

As a Sr. Quality Analyst, you will support the business strategy for LATAM by managing quality oversight of external manufacturing partners. Your responsibilities will include:

• Identifying, evaluating, and recommending potential external manufacturers.

• Ensuring compliance with Quality Agreements and influencing external partners to meet Kenvue's standards.

• Supporting the management of EM procedures and specifications.

• Guaranteeing adherence to Kenvue policies, procedures, quality standards, and applicable safety and environmental regulations.

• Developing solutions to complex database issues and quality-related challenges.

• Creating and updating operating procedures, quality records, and other documentation.

• Monitoring performance trends and recommending improvement opportunities.

• Reporting quality-related risks and insights to management and cross-functional teams.

• Ensuring the release of product batches only when all compliance requirements are met.

• Investigating and tracking quality issues and customer complaints, providing data for quality reports.

What We’re Looking For

We’re seeking a proactive and strategic professional with strong technical skills and the ability to influence across teams and external partners.

Qualifications:

• Degree in Pharmacy, Engineering, or a related field.

• Minimum of 5 years' experience in Quality within the cosmetics or pharmaceutical industry.

• Certified internal or external auditor.

• Solid knowledge of Cosmetic GMP regulations.

• Familiarity with Good Laboratory Practices (GLP) and statistical techniques (preferred).

• Advanced English proficiency (written and spoken).

Key Competencies:

• Strong leadership and ownership mindset

• Ability to influence and negotiate with internal and external stakeholders

• Results-driven, adaptable, and resilient

• Excellent interpersonal and teamwork skills

• Comfort working under pressure in dynamic environments

Be part of a team that’s making a positive impact across the region—apply today and help bring health and wellness to more people every day.

If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.