Global Compliance Information Manager

Global Compliance Information Manager

What we do

At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent.

Who We Are

Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated.  We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. For more information, click here.

Role reports to:

Head of Proactive Reg Comp and Standards

Location:

North America, United States, New Jersey, Skillman

Work Location:

Hybrid

What you will do

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

What’s in it for you

$124,100.00 - $175,200.00

This takes into account a number of factors including work location, the candidate’s skills, experience, education level & other job-related factors.

Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment based on merit without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.