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Senior External Manufacturing Quality Leader

Job in Summit, Union County, New Jersey, 07902, USA
Listing for: Kenvue Inc.
Full Time position
Listed on 2026-08-02
Job specializations:
  • Management
    Regulatory Compliance Specialist
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist
Job Description & How to Apply Below

Kenvueは現在、a:

External Manuf Quality Manager - 2 Roles

私たちがしていること

Kenvueで、日常のケアの並外れた力を実感します。100年以上にわたる伝統を基盤に、科学に根ざした当ホテルは、ニュートロジーナ®、アヴェーノ®、タイレノール®、リステリン®、ジョンソンズ®、バンドエイド®など、すでにお馴染みのアイコニックなブランドを展開しています。科学は私たちの情熱です。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~22,000人の優秀な人々で、すべての声が重要で、すべての貢献が評価される職場文化を持っています。私たちは洞察に情熱を注いでいます。 革新とお客様に最高の製品を提供することに取り組んでいます。専門知識と共感力を持つKenvuerであることは、毎日何百万人もの人々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、熱心に気を配り、科学で信頼を勝ち取り、勇気を持って解決します。そして、素晴らしい機会があなたを待っています!私たちと一緒に、私たちの、そしてあなたの未来を形作りましょう。詳細については here をクリックしてください.

Role reports to:
Senior Manager, Ext Mfg. Quality

Location

North America, United States, New Jersey, Summit

勤務地

ハイブリッド

あなたがすること

The QA Manager, External Manufacturing Quality is primarily responsible for ensuring that 3rd-party organizations who are manufacturing, packaging, controlling, and handling Kenvue products fully understand and meet Kenvue quality and compliance expectations. The NA EM product portfolio consists of both oral ingestible and topical OTC drugs, medical devices, combination products, NDA’s, cosmetics, engineered products, etc. for Kenvue. This position provides risk-based QA direction, perspective, and support to a range of technical, compliance and business issues pertinent to EM products, processes, programs, and activities.

This is a leadership position within the EM quality unit. The position provides key input in the development of strategies, goals, and initiatives, with the authority and responsibility to manage their effective deployment and execution. This position has direct responsibility for a team of professional employees (Quality Leads and Specialists) at multiple levels of experience, training, and skills. The QA Manager is expected to manage team member development, performance, and empowerment consistent with the goals and expectations of Kenvue and the Make Quality organization.

Key Responsibilities
  • Responsible for the performance of a select portfolio of EM sites that may include multiple product classes, technologies, and complexities. Responsible for oversight of quality systems aspects as applicable.
  • Develop, implement, and oversee execution of strategies, plans, and initiatives to ensure production of Kenvue products that consistently meet Kenvue and Health Authority requirements for Quality and compliance.
  • Develop aligned, respectful, and productive relationships with Kenvue and EM peer and leadership partners across multiple responsibility levels and within a high matrix structure. Work with senior leadership to advance the organization and drive improvement.
  • Set reasonable expectations, gain agreement, develop mutually accepted actions, and coordinate execution strategies. React decisively to a wide range of non-conformance events, CAPAs, and other quality/compliance indicators.
  • Drive short and long-term remediation actions that meet requirements and create an improved future state. Provide expertise, oversight, mentoring, and guidance to others, developing expertise and driving decision-making capabilities to lower levels and across functions.
  • Drive system and process improvements to deliver enhanced team performance.
  • Approve the work of others, ensuring quality and compliance to strategies, plans, standards, procedures, and health authority regulations. Review and approve Annual Drug Product Reviews.
  • Lead and/or participate as a key contributor to cross-function, cross region, cross sector teams addressing high complexity/high impact issues, initiatives, and…
Position Requirements
10+ Years work experience
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