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：
Sr. Commercial Quality Specialist位置：
Asia Pacific, South Korea, Seoul, Seoul工作地点：
混合你会做什么
The responsibility of this job is to support the overall operation of Quality function ensuring compliance to Kenvue's global requirements and local regulations for GxP activities in Korea.
[Responsibilities]
Manage the quality inspection and test activities of imported OTC/Q- drug/Cosmetic products including incoming inspection of products and release testing.
Manage QA activities for imported OTC/Q- drug/Cosmetic products release from End to End, incoming inspection, sample shipment arrangement, release checklist preparation and so on.
Oversee the new product introduction process including test method transfer, QC tests, change control management and related documents preparation.
Implement the Quality System via transposition of the requirements of the Commercial Quality procedures.
Execute requirements regarding lifecycle management of GxP related documents and records (creation, approval, distribution, revision, retrieval, retention, disposition) to ensure regulatory compliance and business continuity.
Update and keep GxP documents up to date on EDMS.
Participate in the product performance related issue handling and product nonconformance with collaborating with cross functional quality teams.
Ensure appropriate Change control/Deviation/CAPA/Effectiveness check procedures are followed. Monitor quality records status for timely closure and support issues using QMS.
Ensure a review of the APQRs as required by local regulations.
Support product complaint management.
Support internal audit and HA inspection for auditing and documentation
Support supplier qualification and document management.
What we are looking for
[Requirements]
- Bachelor’s degree or equivalent / Science, Chemistry, Biology, Biochemistry, etc.
- At least 2-4 years of experience preferred in the Pharmaceutical or related industry, ideally with QA & QC operations.
- Fluency in English and Korean (spoken and written)
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