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：
Quality Control Manager位置：
Asia Pacific, South Korea, Seoul, Geumcheon-gu工作地点：
完全现场你会做什么
Laboratory Responsibilities
- To carry out physical and chemical testing as per stipulated timeline & SOP (HPLC, GC, IR, UV, AAS, pH, Viscosity….etc)
- To support receiving finished goods samples and test plan
- To conduct testing equipment maintenance and verification as stipulate in equipment SOP.
- To manage laboratory stock such as chemical reagent, consumables.. etc.
- To ensure all equipment are calibrated for routine analysis.
- To ensure the OOS procedure is strictly followed and compliance.
- To initiate non-conformance/OOS found and assist in non conformance/OOS investigation and support corrective actions to prevent future occurrence
- To ensure that equipment maintenance as per SOP.
- Maintaining good condition of the laboratory, and that the laboratory reflects a high standard of housekeeping.
- To ensure that Good Laboratory Practice is strictly adhered to at all the time.
- To established and monitor the calibration schedule and to ensure lab equipment are adequately calibrated before expiration.
- Follow 5S in lab activities to keep it clean and arranged
Data Integrity
- Follow ALCOA principal for lab activities
Document control related to chemical test result
- Prepare log-book and maintenance it accordingly
GMP and SHE (Safety Health and Environmental) compliance.
- Ensure GMP and SHE requirements are adhered at all the time
- To ensure workstation are clean and orderly
Control and update the reference standard & column for HPLC/GC
- To update the receiving reference standard reagent with expiry date
- To control MSDS and CoA of reagent
- To update column master list
Requirements
Analytical lab experience including HPLC/GC/IR..etc minimum 2-3 years
Knowledge/experience of GMP, Quality Systems, QA/QC compliance & regulation
Good communication skill with people (English skill would be preferred but not mandate)
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