關鍵能力
職缺優勢
工作職責
2.客戶抱怨處理
3.製程品質改善
4.統籌與召開品質會議
5.品質改善活動推展
6.品質標準之制定與審核
7.客戶稽核對應處理
8.人員管理與流程規劃
理想人選
其他條件
科系:不拘
年資:5年以上工作經驗
出差外派:無需出差外派
公司福利
關鍵能力
職缺優勢
工作職責
理想人選
其他條件
公司福利
1. 制定產品開發計劃,領導研發團隊進行新產品概念發想、配方開發、原料選擇、生產流程設計和包裝設計等工作。
2. 建立有效的品質控制流程,確保公司產品在生產過程中和市場上的品質一致。
3. 確保公司產品符合相關法規和標準,包括食品安全、營養標示和包裝要求等。
4. 有效管理研發項目,控制成本並優化資源使用,達成研發目標。
5. 關注市場趨勢和競爭對手動向,了解消費者需求和市場變化,確保公司產品能夠保持競爭力並滿足市場需求。
6. 培育研發團隊的專業職能成長、協作和創新,確保團隊在食品研發領域保持競爭力。
1. 15年以上製造業OEM/ODM工作經驗,5年以上高階營運經驗
2. 需有熟悉如何管理製造大廠,廠規模至少千人以上,歷練過生產高階or業務高階or營運高階
3. 管理業務/生產/財務/QA/採購/HR/ME等單位
4. 需對數字相當敏銳,業績達成率/財報分析/成本分析/營運利潤分析,並提供過往相關數字成效
5. 策略推廣與執行,業務擴張達成營運目標,推展未來3-5年營運計畫,並有實際執行經驗
6. 英文需聽說讀寫精通,能流暢直接對應國際品牌客戶端
7. 過往需有跨國文化的管理經驗,管理過多國文化員工,並能激勵團隊
8. 此職務需在越南/印度等大廠歷練,能接受長期於東南亞
1. Plan, implement and coordinate activities related to quality system, quality assurance, quality verification, customer problem handling and daily management of the department.
2. Collection and update of domestic/foreign medical device regulatory certifications and related regulations and standards.
3. ISO13485 and GMP quality system audit related matters.
4. Matters related to domestic/foreign medical device clinical trials.
1. Quality control: Advanced review work of the NPI process, supervising the compliance of suppliers, assessing quality risks in product development and mass production introduction; assisting department heads in reviewing various quality-related agreements
2. Supplier management: Lead the recognition, assessment and regular review and coaching of suppliers by various departments; review the evaluation data of new materials, new suppliers and foundries; lead the communication of the company's various engineering change needs to the foundries , and track and confirm the evidence and information provided by the foundry to assess risks
3. Environmental protection control: supervise the various OEM processes and product environmental compliance of the foundry, supervise the procurement department to communicate the requirements for environmental management substances (environmentally banned substances) to external suppliers, and confirm the evidence and information provided by extern