Kenvue 目前正在招聘 a：
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：
自我护理高级QA经理位置：
Asia Pacific, China, Shanghai, Shanghai工作地点：
完全现场你会做什么
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.
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