Sr. Quality Analyst – Fixed term role 1 year
- Función del trabajo:
- Fecha de publicación:
- Fecha de finalización:
- ID:
- 2507037194W
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Lo que hacemos
En Kenvue, nos damos cuenta del extraordinario poder del cuidado diario. Sobre la base de más de un siglo de herencia y arraigados en la ciencia, somos el hogar de marcas icónicas, incluidas NEUTROGENA®, AVEENO,® TYLENOL,® LISTERINE,® JOHNSON'S® y BAND-AID® que ya conoces y amas. La ciencia es nuestra pasión; El cuidado es nuestro talento.
Quiénes somos
Nuestro equipo global está formado por ~ 22.000 personas brillantes con una cultura laboral en la que cada voz importa y cada contribución es apreciada. Nos apasionan las ideas, innovación y comprometidos con la entrega de los mejores productos a nuestros clientes. Con experiencia y empatía, ser un Kenvuer significa tener el poder de impactar a millones de personas todos los días. Ponemos a las personas en primer lugar, nos preocupamos ferozmente, nos ganamos la confianza de la ciencia y resolvemos con coraje, ¡y tenemos oportunidades brillantes esperándote! Únase a nosotros para dar forma a nuestro futuro y al suyo. Para obtener más información, haga clic en aquí.
Role reports to:
GER GAR QA SRUbicación:
Latin America, Argentina, Buenos Aires, PilarLugar de trabajo:
HíbridoWhat will you
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.
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