Senior Manager, Quality Systems

Senior Manager, Quality Systems

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：

Director NA Quality Excellence

位置：

North America, United States, New Jersey, Summit

工作地点：

混合

你会做什么

The Senior Manager, Quality Systems is responsible for driving end‑to‑end (E2E) quality systems oversight and ensuring the effectiveness of processes across the North America Quality & Compliance organization. This role provides strategic leadership and operational guidance across regional, functional, and site-level teams, fostering a culture of quality excellence and continuous improvement. The successful candidate will demonstrate strong, influential leadership and the ability to inspire new ways of thinking, working, and collaborating across the Quality Organization. The Senior Manager will translate global and regional quality strategies into actionable plans for North America. This position will serve as a critical liaison to North American sites and cross-functional partners, ensuring regional needs are represented and integrated into global processes and initiatives.

As a core member of the Quality Systems team, the Senior Manager will also contribute to both strategic and operational activities that sustain and advance quality and compliance across the base business. This includes supporting the design, implementation, and governance of quality systems, enabling the organization to meet regulatory requirements, strengthen operational discipline, and enhance overall quality maturity.

Responsibilities:

• • Demonstrated track record in developing, implementing, and sustaining efficient and effective Quality System processes.

  • Proven success in building strong cross‑functional partnerships and collaborating effectively across diverse stakeholder groups.

  • Experience working with virtual and geographically dispersed teams to drive aligned execution.

  • Strong working knowledge of Quality System elements, including Metrics, Audits, Regulatory Standards, and general Quality Systems processes.

  • Experience serving as organizational and functional expertise during Health Authority inspections and internal audits.

  • Extensive experience with GMP/GxP requirements and their application in a regulated manufacturing environment.

  • Thorough understanding of cGMPs for prescription and over‑the‑counter products, including systems used to support their deployment.

  • Strong influencing skills with the ability to engage and guide leaders, peers, and teams without direct authority.

  • Excellent written and verbal communication skills, with the ability to tailor messages across levels and functions.

  • Demonstrated ability to lead and deliver complex, cross‑functional projects with strong execution discipline and sustained results.

  • Lead the sustainment of core processes and guidelines and contributes to improvement initiatives, including decision-making, recruitment, resource planning, budget oversight, and performance management.

  • Develop talent and build team capabilities to meet future business demands, while providing ongoing mentoring and coaching to support employee growth and performance.

  • Broad and in‑depth experience across core Quality Assurance functions, with a solid understanding of end‑to‑end quality principles and practices.

  • Proactively evaluate Quality Management System trends and drive the development and implementation of action plans.

  • Strong systems thinking mindset with advanced analytical, technical, problem‑solving, and organizational skills to assess issues, identify solutions, and drive improvements.

  • Serves to drive change by championing the implementation and sustainment of processes and systems that align with the evolving regulatory environment.

  • Ability to communicate effectively with Subject Matter Experts (SMEs), decision makers, and key stakeholders at both regional and global levels, tailoring messages appropriately and facilitating alignment.

Required Qualifications:

• Education: A minimum of a Bachelor's degree is required with a focus in Life Sciences, Engineering, or related field: Master's or Advance degree is preferred.

• A minimum of 5-10 years experience in the field of Quality Systems and Compliance, Project Management, and in an FDA regulated industry (Medical Device, OTC, Cosmetics).

• A minimum of 3 years of People leadership experience required.

• This position may require up to 20% domestic travel as required by business needs.

Preferred Qualifications:

• Advanced Degree (MA, MS, MBA)

• Experience with Project Management (PMP or FPX Certification)

• Experience preparing for, supporting, and representing the organization during Regulatory Inspections and interactions

• Excellent knowledge of procedures governing an FDA Regulated Industry

#LI-MA1

对您有什么好处

$153,850.00 - $217,200.00

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。