轉職熱搜工作

1.纖維基材與PU之人工皮革複合材料技術開發，進行設計與材料測試。 2.分析製程異常，制定改善計畫與實施效能優化策略。 3.執行製程實驗，整理實驗數據並撰寫分析報告。 4.負責跨部門協作，確保項目完成與技術應用實踐。 5.儲備幹部經錄取後，將視廠區人員需求安排實習工作，並依表現及職缺進行分發。 6.透過學習部門間組織運作及培養溝通協調能力，加速了解各項工作執行方式及相關細節。 7.培養有效執行能力，完成各項主管交辦事項。 8.試用期間派駐海外另有海外實習津貼，正式派駐後另依據表現核定薪資。 9.正式派駐後年薪約950,000元(視浮動獎金水平)。

1. 生產作業執行 (投料/洗桶/充填/包裝) 2. 生產環境維護 3. 生產設備保養點檢 4. 主管交辦事項 5. 可配合平日/假日加班 6. 可接受著無塵衣及無塵室作業 7. 可接受有機溶劑味道 8. 可配合早班(07:30~16:30)、常日班(08:30~17:30)、 小夜班(15:00~24:00)輪調 ※需搬重物。

1. Review and provide the technical recommendations for CMC documentation and Common Technical Document(CTD) dossier from a regulatory perspective. 2. Interpretation and Handling the regulatory technical query’s responses that were asked by Client and Authority during the due diligence or submission deficiency phase and provide the action plan or solution and scientific justification. 3. Responsible for evaluating the registration feasibility and mapping the global registration strategy for assigned new R&D products. 4. Cooperate and teamwork with R&D, technical, and RA PM on new R&D project technical challenges and complete the dossier till product approval. 5. Responsible for regulatory registration for export products and make sure all the documents are meet the authority‘s requirements. 6. Responsible for deficiency response preparation to ensure our response meets the authority’s requirements. 7. Accurately follow the update of the registration regulation, and provide the regulation update to the team and training.

1. 協助產線PCN打樣、試車、量產、廢水排放、6S、產線建置 2. 生產環境維護 3. 生產設備保養點檢 4. 主管交辦事項 ※需至台南廠(台南樹谷園區)短期實習三個月。 ※具堆高機經驗佳。 ※需搬重物。

1.執行疫苗或其他藥品無菌調劑/配製製程 2.生產線設備準備與操作、例行驗證與確效、第一級預防保養執行 3.作業環境無菌相關準備維護 4.原物料、設備等製程相關請領作業 5.修訂GMP規範相關文件與定期審閱 6.其他主管交辦事項 職缺頁面所列工作待遇為核定薪資 另有其他獎金、津貼，依實際工作狀況於核定薪資外另計（如排班津貼、職場津貼等） 並依生產狀況另提供生產津貼 上述獎金、津貼依公司規範章程現況為主

1.監督承包廠商工程的執行進度與施工品質。 2. 具識圖及實際施工能力。 2.業主、廠商的溝通協調。 3.驗收工程與結算。 4.維持廢水廠操作之穩定。 5.其他主管交辦事項。 (大學以上畢業具相關科系及2年以上相關工作經驗佳)

1.開發調整分析方法(HPLC, GC, IC...)，協助產品製程開發，分析方法之確校 2.執行實驗室設備3Q 3.研擬審查藥典相關產品規格及分析測試，建立藥典規格 4.操作化學分析儀器進行分析，協助產品放行

1. Support and facilitate business user‘s requirement to seamlessly running at corporate SAP system in the landscape via analyzing, designing, and developing. 2. Work closely with the team (other SAP developers, infrastructure & system teammates) to understand business needs and deliver features in good quality at timely manner. 3. Be capable of creating and assessing software architecture/designs with multiple stakeholders. 4. Manage overall change request and/or incident backlog for the owned topics and ensure the high quality of corrections and notes for the owned topic areas and of stable assist packages with no regressions. 5. Exhibit learning agility by quickly upskilling on new tasks and concepts. 6. Assist our business users during product deployment, critical operations, and system rollout via standard infrastructure, creating maintenance notes and documentation. 7. Will be providing presentations and workshops.

1.協助主管規劃廠房、設備、生產、Artwork、品質制度等運作落實，以提昇部門績效。 2.協助各類專案之規劃與執行。 3.完善人才培訓體系及晉升發展管道。 4.100％藥廠CGMP訓練。

1. Review and enforce adherence to quality standards and agreements. 2. Manage non-conformance investigations and compliance. 3. Oversee GMP and regulatory compliance. 4. GMP Supplier Oversight: -Oversight the GMP Vender Audit Schedule. Ensuring Vendor and Auditor availability (internal/external/consultant) and confirming audit dates with both auditors and vendors. -reviewing supplier audit reports, ensuring they meet Lotus QA Standards and are compliant with Lotus SOPs. -Submitting observation reports to vendors, communicating response timelines and tracking them to ensure timely responses. Review of vendor audit responses and managing the review/editing cycle until responses are acceptable. Requesting documented evidence of closure when necessary and filing electronically and hard copy. 5. Manage quality assurance tasks including document control and investigations.