Kenvueは現在、以下求人を募集しております。
Quality Control Analyst (계약직)私たちがしていること
私たちKenvueは、日々のケアが持つ驚くべき力を信じています。100年以上の伝統と科学に根ざし、Neutrogena®, Aveeno®, Tylenol®, Listerine®, Johnson’s® and BAND-AID®など、皆様が既にご存じでご愛用いただいているアイコニックなブランドを提供しています。科学は私たちの情熱であり、ケアは私たちの才能です。
Who We Are
私たちのグローバルチームは、インサイトとイノベーションに情熱を注ぎ、最高の製品をお客様にお届けすることに全力を注ぐ、多様で優秀な22,000人以上の社員で構成されています。専門知識と共感力を備えたKenvuerであることは、毎日何百万人もの人々の生活に影響を与える力を持つことを意味します。私たちは、人を第一に考え、全身全霊をもってケアし、サイエンスで信頼を獲得し、勇気をもって解決します。私たちとあなた自身の未来を、共に切り開いていきましょう。
Role reports to:
Quality Control Manager場所:
Asia Pacific, South Korea, Seoul, Geumcheon-gu勤務地:
フルオンサイトあなたがすること
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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