Senior Compliance Auditor

Kenvue

5d•Onsite

About The Position

Kenvue is currently recruiting for a: Senior Compliance Auditor 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: COMPLIANCE MANAGER Location: North America, United States, Puerto Rico, Las Piedras Work Location: Fully Onsite What you will do The Senior Compliance Auditor is responsible of the Internal Audit Program. May work as lead auditor during some internal audits as established in the schedule. Presents internal audits findings with the classification to the audited department manager, evaluate responses, and follow up action items until they are completed and documented. Assists with the management of inspection readiness activities, regulatory (FDA, DEA) and pre-approval inspections.

Requirements

Bachelor degree in Finance, Accounting Business or any related field.
Minimum 5 years of experience working in compliance, auditing, regulatory affairs or quality roles.
Experience in companies regulated by FDA, pharmaceutical or OTC sectors.
Minimum of 2 years of experience in GMP auditing.
Experience handling regulatory agency, internal and external audits, investigations, Statistic, manufacturing processes, and report preparation.
Experience in quality metrics: collection, analysis, trends, signals and reporting.
Knowledge of cGMP 21, CFR Parts 11, 210 and 211, Europe, Asia and Canada regulations.
Computer literate (MS Office, Pulse. SAP, MES, Pulse, ETQ, etc.).

Nice To Haves

Master’s Degree in Accounting, Finance, Business Administration, Quality Management, or a related field (preferred).
ASQ Certified Quality Auditor (CQA) or equivalent certification in auditing and compliance.
Fully bilingual (English and Spanish) with excellent written and verbal communication skills.

Responsibilities

Lead and execute internal audits across operational, financial, and compliance areas.
Ensure adherence to corporate policies, regulatory standards, and risk management frameworks.
Prepare audit reports and oversee corrective action implementation.
Conduct regular Good Manufacturing Practice (GMP) walkthroughs in production and packaging areas.
Develop, track, and report compliance and audit-related metrics (e.g., audit completion rates, CAPA effectiveness.
Perform compliance audits and investigations of suppliers and third-party manufacturers.
Establish KPIs for compliance programs and audit performance.