Summer Intern, Operations

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

Job Summary: The QA Summer Intern will support the Quality Assurance team in reviewing and organizing applicable pharmaceutical regulations, internal quality procedures, and product release process requirements. This role is designed for a student who is interested in pharmaceutical quality systems, GMP compliance, and batch/product release activities in a manufacturing environment. The intern will assist in mapping regulatory requirements to site procedures, summarizing key compliance expectations, and helping improve the clarity and efficiency of product release related documentation and workflows.

Key Responsibilities:
• Review and summarize applicable pharmaceutical regulations, GMP requirements, and internal SOPs relevant to QA operations and product release.
• Support the compilation and organization of regulatory requirements related to batch review, product disposition, and release decision making.
• Assist in mapping the end-to-end product release process, including key inputs, review points, approval steps, and associated documentation.
• Help prepare process flowcharts, summary tables, and training materials for QA use.
• Compare regulatory requirements with current site practices and help identify gaps, inconsistencies, or opportunities for clarification.
• Support document review, data collection, and tracking of action items related to release process improvement.
• Participate in cross-functional discussions with QA, Production, QC, and Regulatory Affairs when needed.
• Perform other QA support activities assigned by the supervisor.

Qualifications:
• Bachelor’s degree candidate or postgraduate student in Pharmacy, Pharmaceutical Engineering, Chemistry, Biology, Quality Management, or other related discipline.
• Strong interest in pharmaceutical manufacturing, GMP compliance, and quality systems.
• Good reading and comprehension skills for English regulatory and technical documents.
• Good written and verbal communication skills in English.
• Strong attention to detail, logical thinking, and document organization skills.
• Proficient in Microsoft Office applications and AI tools.

Preferred Skills:
• Basic knowledge of GMP, pharmaceutical regulations, or quality assurance processes.
• Ability to summarize complex requirements into clear and practical language.
• Ability to work independently while maintaining good teamwork and communication.

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