コンテンツにスキップ
採用情報に戻る

Sr. Quality Analyst – Fixed term role 1 year

職務分類:
掲載日:
終了日:
ID:
2507037194W

この仕事を共有する:

Kenvueは現在、以下求人を募集しております。

Sr. Quality Analyst – Fixed term role 1 year

私たちがしていること

私たちKenvueは、日々のケアが持つ驚くべき力を信じています。100年以上の伝統と科学に根ざし、Neutrogena®, Aveeno®, Tylenol®, Listerine®, Johnson’s® and BAND-AID®など、皆様が既にご存じでご愛用いただいているアイコニックなブランドを提供しています。科学は私たちの情熱であり、ケアは私たちの才能です。 

Who We Are

私たちのグローバルチームは、インサイトとイノベーションに情熱を注ぎ、最高の製品をお客様にお届けすることに全力を注ぐ、多様で優秀な22,000人以上の社員で構成されています。専門知識と共感力を備えたKenvuerであることは、毎日何百万人もの人々の生活に影響を与える力を持つことを意味します。私たちは、人を第一に考え、全身全霊をもってケアし、サイエンスで信頼を獲得し、勇気をもって解決します。私たちとあなた自身の未来を、共に切り開いていきましょう。 

Role reports to:

GER GAR QA SR

場所:

Latin America, Argentina, Buenos Aires, Pilar

勤務地:

ハイブリッド

あなたがすること

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.

障害のある個人の方は、宿泊施設のリクエスト方法について障害支援ページを確認してください。