1.Perform process validation in accordance with company and regulatory requirements. 2.Prepare and revise production Master Batch Record for process validation and commercial. 3.Execute manufacturing process. 4.Prepare data summary and reports. 5.Other duties as assigned, such as shipping study, bulk hold study, and packaging validation.
待遇面議
(經常性薪資達 4 萬元或以上)
1.B.S. /M.S. degree in Pharmaceutical Sciences, Chemistry, or Chemical Engineering preferred with 0-2 year experiences. 2.Strong problem solving, communication skills and attention to details are essential. 3.Good written and oral communication skills are required. 4.Must be well organized, detailed oriented and able to multi-task. 5.Hands on experience in operating lab and manufacturing equipment is a plus. 6.GMP knowledge/experience is a plus. 7.Good reading and writing in English,fluent speaking in English is a plus.
益邦製藥提供與美國製藥大廠一致規格的辦公與製造工作環境,從設計到建造皆聘請國內外專業團隊精心規劃,以結合機能性的空間動線,充份詮釋益邦製藥堅守符合世界級品質要求之經營策略。 *具競爭力的薪資水準 *每年依據績效/市場薪資調查結果調薪 *優於勞基法的休假制度 *免費提供用餐、現磨咖啡機及飲料機 *免費員工停車位 *員工/眷屬團保 *年度員工健檢 *年度員工旅遊 *三節禮金禮卷 *多元化社團活動 *員購優惠