Officer - R&D Quality

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.

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What you will do

Officer - R&D Quality

Job Purpose

Responsible for ensuring Quality Management System (QMS) compliance across R&D laboratories and external service providers through management of laboratory investigations (OOS/OOT), stability programs, supplier quality activities, training compliance, documentation control, computer system validation, and quality metrics reporting. Supports regulatory compliance, inspection readiness, and continuous improvement initiatives within the R&D organization.

Key Responsibilities

• Reviewing Quality documents such as change controls, method validations, test methods, technical justifications, and periodic reviews.
• Managing stability programs to ensure studies are executed, monitored, and documented in compliance with quality requirements.
• Supporting laboratory investigations, including review of OOS/OOT events, root cause analyses, corrective actions, and retest evaluations.
• Overseeing laboratory compliance activities, conducting compliance assessments, supporting Gemba walks, and maintaining audit and inspection readiness.
• Managing supplier qualification processes, supplier audits, approved supplier lists, and supplier corrective action programs.
• Serving as the site training coordinator, monitoring training compliance, managing training systems, and reporting training metrics.
• Supporting computerized system validation activities, including review of validation documentation and periodic system assessments.
• Preparing and reporting quality metrics related to investigations, CAPAs, audits, training, and compliance performance.

Qualifications & Experience

• Bachelor’s or master’s degree preferably in Microbiology, other preferences are Biotechnology, Pharmacy, Chemistry, Life Sciences, or a related scientific discipline.
• Minimum 4 years of Experience in Quality Assurance, Quality Control, R&D Quality, or regulated laboratory environments.
• Working knowledge of GMP, GLP, laboratory investigations, CAPA, change control, supplier quality management, and computerized system validation.
• Experience with electronic quality management systems and document management platforms preferred.
• Exposure to regulatory audits like USFDA & EUGMP

If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.