Director, Quality & Compliance

Director, Quality & Compliance

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：

Sr Director NA MAKE Q and C

位置：

North America, United States, Pennsylvania, Lititz

工作地点：

完全现场

你会做什么

Accountable to provide leadership and to guide and manage the Quality activities to assure that all products produced at Lititz meet company and regulatory standards.  Lead Good Manufacturing Practice (GMP) compliance efforts and assure alignment with regulatory compliance systems and Kenvue procedures. Develop the organization’s strategies, goals and objectives in accordance with company’s strategy.

Key Responsibilities

• Directs the implementation and administration of quality management systems in accordance with applicable standards
• Oversees the development and implementation of processes, procedures, audits and corrective actions.
• Ensures effective communication and training are deployed throughout the business.
• Primarily at a Local and Regional Level.
• Provides overview or detailed communications to Q&C and cross-functional leadership on status of initiatives and issues.  This communication occurs at a plant-level, and occasionally at a regional-level.
• Is accountable to deliver a broad range of safety, quality and customer service metrics at the plant level, through individual and team execution. 
• Develops tactics to ensure successful delivery of goals, securing resources and identifying accountability.
• Is knowledgeable to execute quality systems including risk management, investigations, change control and CAPA. 
• Has a working knowledge of at least one other system including production, packaging and labeling, facilities and equipment, materials or laboratory controls.
• Troubleshoots and solves high risk and high complexity issues, using experience, ingenuity and creativity to implement solutions across a wide range of root causes.
• Lead the design and implementation of safety, Q&C, customer service and cost improvement programs and initiatives.  Innovate solutions to significant quality system gaps and lead continuous improvement projects.
• Is accountable for product disposition and compliance decisions at the plant level.  Escalates when required by procedure, or when potential impact to safety, systemic compliance, customer service or at significant cost.
• Assures compliance with all local government regulatory requirements and requirements related to things such as sampling plans, design control, and quality systems.
• Develops initial and subsequent modifications of product assurance programs to delineate areas of responsibility, personnel requirements, and operational procedures within program.
• Organizes, plans, leads and manages quality related projects in alignment with company goals.
• Monitors supplier quality related activities to assure fulfillment of contract/purchase order requirements.
• Facilitates the development and training of immediate staff.
• Primary point of contact with all health authorities.
• Cultivates a culture of quality, acting as the voice of Q&C during plant-level interactions. 
• Has a high degree of shop-floor presence (when applicable – might be QA 26 or Lab 26); is visible to employees at all levels of the plant organization as a Q&C leader
• Identifies, supports assessment and documentation of issues that might pose compliance risks, supporting investigation and solutions, actions and recommendations in case of QRB and Escalations.
• Identifies, recruits and develops high-performing talent. 
• Ensures a strong pipeline of talent for critical positions. 
• Manages performance of direct reports, and provides input to talent processes for other individuals in the Q&C organization

What we are looking for

Required Qualifications

• Minimum degree in Science / Engineering or related discipline .
• A minimum of ten (10) years of GMP experience (or seven (7) years of experience in a QA role, with plant QA experience preferred) in either Pharmaceutical, Medical Device, OTC Drug, Cosmetic and/or Food and Dietary Supplements Production

Desired Qualifications

• Master’s Degree in Engineering / Science / Administration (In Supply Chain/Business) considered an asset
• Expert knowledge of cGMP requirements and current Health Authority (i.e. FDA, ANVISA, Health Canada, MHRA) enforcement issues across multiple regulatory classes (Rx, OTC, Cosmetic, Medical Device).
• Demonstrated ability to lead cross-functional local teams, and participate in regional teams to accomplish business objectives, enhance relationships, and inform management to drive change and provide direct feedback.
• Demonstrated ability to work on complex or ambiguous issues autonomously, with little/no daily direction.

#LI-MA1

对您有什么好处

$190,825.00 - $269,400.00

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。