Global Compliance Information Manager

Global Compliance Information Manager

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：

Head of Proactive Reg Comp and Standards

位置：

North America, United States, New Jersey, Skillman

工作地点：

混合

你会做什么

Global Compliance Information Manager

The Global Compliance Information Manager provides compliance data analytics for the Kenvue Quality, Compliance & Excellence organization. This position will monitor the global regulatory environment for changing regulations and health authority trending. In addition, this role is responsible for preparing routine department reports/updates, providing as needed metrics, managing compliance data trends, maintaining training, and identify/implement process and data quality improvement opportunities. This position will work closely with the VP, Kenvue Quality, Compliance & Excellence, Regional Compliance Leads, Kenvue Quality Systems, and Kenvue Regulation Management in areas related to compliance data and emerging regulatory trends and requirements.

• Collect, analyze, and report global compliance data, including data from Kenvue compliance and quality programs for the following forums:

• • QHS Regulatory compliance updates

  • Global Kenvue quality management review

  • Kenvue Leadership Team and Kenvue Board of Directors reporting

  • Kenvue’s Healthy Lives Matter public reporting

• Ad hoc compliance data trending and reporting for the Global Quality, Compliance & Excellence team

• Monitor relevant quality and compliance forums for hot topics and trends both internally (e.g., regulatory compliance data system of record) and externally (e.g., health authority websites/reports, industry monitoring tools).

• Develop and issue summary report(s) on compliance information and trends that impact Kenvue businesses.

• Maintain department periodic reporting.

• Maintain Quality, Compliance & Excellence department processes, data, information, and training.

• Support Kenvue regulatory compliance audits/follow-up and inspection readiness

• Support Quality, Compliance & Excellence team project initiatives

Required Qualifications

• Bachelor’s degree in science (e.g., Biology, Chemistry or related field)

• 8+ years of experience in Quality Assurance, Regulatory Affairs, Compliance and/or other related areas in a matrixed Life Sciences (Consumer, Pharmaceutical and/or Medical Device) organization

• Hands-on experience with quality system and compliance reporting (i.e. data analytics and trending)

• Working knowledge of FDA and equivalent Health Authority GMP regulations

• Exceptional organization skills  

• Meticulous attention to detail in reporting with the ability to anticipate obstacles and barriers and mitigate these issues

• Excellent communication skills, with the ability to articulate and express concepts clearly and persuasively both verbally and in writing, particularly when simplifying complex regulatory or technical issues

• Ability to work autonomously as a high impact individual contributor and manage multiple priorities and deadlines in a fast-paced environment  

• Working knowledge of compliance and quality systems and tools (e.g., Curve, ETQ, Veeva, Tableau)

• Proficiency with MS Excel

• Travel: ~10% travel

Desired Qualifications

• Understanding of regulatory bodies approach to inspections and how to respond to regulatory body observations

• Experience preparing reports and/or data summaries for varying audiences

对您有什么好处

$124,100.00 - $175,200.00

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。