Quality Excellence Lead

Quality Excellence Lead

我们做什么

在 Kenvue，我们意识到日常护理的非凡力量。我们以一个多世纪的传统为基础，植根于科学，是标志性品牌的品牌 - 包括您已经熟悉和喜爱的 NEUTRGENA®、AVEENO、TYLENOL®®、LISTERINE®、JOHNSON'S® 和 BAND-AID®。科学是我们的热情所在;关心就是我们的才能。

我们是谁

我们的全球团队由 ~ 22,000 名才华横溢的员工组成，他们的职场文化中，每个声音都很重要，每一个贡献都受到赞赏。 我们热衷于洞察， 创新并致力于为我们的客户提供最好的产品。凭借专业知识和同理心，成为 Kenvuer 意味着每天有能力影响数百万人。我们以人为本，热切关怀，以科学赢得信任，以勇气解决——有绝佳的机会等着您！加入我们，塑造我们和您的未来。有关更多信息，请单击 here.

Role reports to：

Dir MAKE Q and C Lititz Site

位置：

North America, United States, Pennsylvania, Lititz

工作地点：

完全现场

你会做什么

Kenvue Lititz Plant develops and markets consumer healthcare, baby care, and beauty/skin care products for consumers and healthcare professionals, incorporating the latest innovations. Its portfolio includes trusted brands such as Listerine, Neosporin, Polysporin, Benadryl, Desitin, Johnson’s Baby Oil, Lubriderm, Aveeno, and Bengay.

The Quality Excellence Lead will drive quality leadership and mentor the Quality Assurance team through transformation initiatives and process excellence strategies. This role ensures integrity, timely execution of tasks, and accountability for compliance and financial metrics, delivering measurable improvements through projects and Continuous Improvement Plans (CIPs) aligned with the Kenvue Production System.

As a change agent, the Quality Excellence Lead will champion innovative, efficient processes and capability-building strategies to support site transformation and future vision. Responsibilities include developing and implementing New Product/Transfer Introduction strategies, policies, and programs that enhance quality, compliance, cost efficiency, and supply chain performance. The role requires monitoring key metrics to ensure new, transferred, and existing products meet Kenvue global standards, U.S. regulatory requirements (including 21 CFR 210 & 211), and continuous improvement goals.

Key Responsibilities

• Lead Quality Frameworks: Develop and implement advanced quality improvement programs aligned with Six Sigma, Lean, and Design Excellence methodologies.
• Manage Team: Supervise quality team, assign work, conduct performance reviews, and design solutions to optimize processes and maintain high standards.
• Drive Audits & Inspections: Conduct data-driven audits and inspections using analytics to identify trends, ensure compliance, and foster continuous improvement.
• Analyze Deviation Data: Address quality deviations and process failures promptly, ensuring effective corrective and preventive actions.
• Mentor & Inspire: Guide team members, including Six Sigma belts, to adopt innovative problem-solving and promote a culture of quality and engagement.
• Collaborate Strategically: Partner with senior leadership to implement forward-thinking quality strategies that meet market, technology, and regulatory demands.
• Approve Changes: Oversee documentation and process changes impacting product quality, ensuring readiness for regulatory audits.
• Monitor & Improve: Analyze production deviations and trends to drive improvement initiatives.
• Train & Educate: Support creation of site-wide GMP training to reinforce compliance and quality awareness.

What we are looking for

Required Qualifications

• Bachelor’s degree (or equivalent) in Engineering, Quality Management, or a related technical/scientific field.
• At least 6 years of experience in a GMP product manufacturing environment, with strong knowledge of quality, compliance, supply chain, and manufacturing operations
• Strong foundation in analytical and strategic thinking.
• Proven ability to lead and influence cross-functional teams using a collaborative leadership style.
• Proficiency in relevant technology and software for quality management and process improvement
• Strong communication and interpersonal skills.
• Strong analytical, problem-solving, and decision-making skills.
• Up to 10% travel

Desired Qualifications

• Proficiency in leveraging modern quality management tools, applications, and software to drive decision-making and operational improvements.
• Exceptional leadership skills with the ability to inspire teams to embrace change and pursue excellence through creative methodologies.
• Experience in coaching and developing talent is preferred.
• Demonstrated expertise in managing quality systems design, regulatory compliance, and process improvement methodologies such as Six Sigma and Lean.
• Excellent written and verbal communication skills capable of conveying complex technical information effectively to diverse audiences.
• Willingness and ability to travel domestically and internationally as required to support quality initiatives and audits.
• Track record of innovative process enhancements.
• ASQ CQA, CQE or CQM certification is preferred

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对您有什么好处

$110,500.00 - $156,000.00

这考虑了许多因素，包括工作地点、候选人的技能、经验、教育水平和其他与工作相关的因素

Kenvue 很自豪能成为一个机会均等的雇主。所有合格的申请人都将根据业绩获得就业考虑，不分种族、肤色、宗教、性别、性取向、性别认同、年龄、国籍或受保护的退伍军人身份，并且不会因残疾而受到歧视。