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我們做什麼
在 Kenvue，我們意識到日常護理的非凡力量。我們以一個多世紀的傳統為基礎，植根於科學，是標誌性品牌的品牌 - 包括您已經熟悉和喜愛的 NEUTRGENA®、AVEENO、TYLENOL®®、LISTERINE®、JOHNSON'S® 和 BAND-AID®。科學是我們的熱情所在;關心就是我們的才能。
我們是誰
我們的全球團隊由 ~ 22,000 名才華橫溢的員工組成，他們的職場文化中，每個聲音都很重要，每一個貢獻都受到讚賞。 我們熱衷於洞察， 創新並致力於為我們的客戶提供最好的產品。憑藉專業知識和同理心，成為 Kenvuer 意味著每天有能力影響數百萬人。我們以人為本，熱切關懷，以科學贏得信任，以勇氣解決——有絕佳的機會等著您！加入我們，塑造我們和您的未來。有關更多資訊，請按兩下 here.
Role reports to：
Quality Control Manager位置：
Asia Pacific, South Korea, Seoul, Geumcheon-gu工作地點：
完全現場你會做什麼
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)
如果您是殘障人士，請查看我們的 殘障人士援助頁面瞭解如何申請便利
