- Singapore
工作地点
职位描述
岗位职责
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Company Profile:
Takeda's Singapore biologics manufacturing facility focuses on manufacturing potentially life-saving medicines for patients suffering from rare blood disorders such as Hemophilia A and B. As part of the company’s Biologics Operating Unit network, the site is Takeda’s only biologics drug substance manufacturing facility in Asia. The facility has two buildings, including manufacturing suites and laboratories, as well as Takeda’s first positive energy building certified by Singapore’s Building and Construction Authority’s Green Mark scheme in 2022.
This position is required perform all tasks associated with the QC analytical lab operations which include chemical analysis, biochemical analysis, equipment calibration/maintenance, records review, records approval, deviation/investigation write up/review, equipment qualification, method validation, method transfer and other tasks as assigned.
Core Responsibilities:
• Act as a Subject Matter Expert (SME) to provide technical advice to QC Personnel in laboratory related troubleshooting e.g. lab equipment failure, method • Provide appropriate training for the QC Analytical Team.
General Responsibilities:
Key Skills and Competencies:
o Organization and planning skills
o Analytical and Logical thinking skills
o Ability to work and collaborate within the team
o Has substantial knowledge and understanding in terms of regulatory standards requirements e.g. USP, EP, 21CFR, ICH etc. o Knowledge in Ion Chromatography (IC), High Performance Liquid Chromatography (HPLC), Fluorescence spectrometer (FLS), pH, Conductivity, Gel electrophoresis (SDS Page or Western Blot), Potency and ELISA
o Knowledge in Empower and LIMS. o Knowledge in Microsoft Office.
o Solves problems and implements corrective actions using six sigma tools.
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