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生產經理S3

蘇州碧迪醫(yī)療器械有限公司

蘇州

無要求
無要求
01-18 發(fā)布

職位信息

職位名稱：生產經理S3

類別名稱：

職位描述：

KEY RESPONSIBILITIES（主要職責）1.Supervises employees in the area day-to-day manufacturing operations.日常管理生產運作的所有生產員工2.Responsible for hiring (with HR input), training, performance evaluation and discipline of employees supervised.負責招聘（與HR合作），培訓，業(yè)績考核以及監(jiān)管所有生產員工的紀律3.Maintains a variety of production records and documents to reflect schedules, performance and procedures.維護多種的生產記錄和文件，以適應時間，業(yè)績和程序的改變4.Generates effective communications, good relations, and a positive image with inside customers, suppliers and coworkers, promoting courtesy, objectivity, fairness and teamwork.具備有效的溝通，良好的關系，與內部顧客，供應商以及合作方打交道，保持謙恭有禮，明確目標，公平和團隊合作形象5.Ensure that accurate and complete records of department activities are kept, and that they meet regulatory requirements.確認準確和完整的部門工作記錄，并保留記錄。所有記錄符合法務要求6.Develop and monitor production schedules, staffing requirements and budgets. Manage implementation of new processes; technologies, or tolling needed to manufacture products.發(fā)展和監(jiān)管生產時間，與員工發(fā)展要求以及預算。管理好新的流程，技術和生產消耗7.Facilitate a team based manufacturing environment按照生產環(huán)境需求發(fā)展生產團隊8.Support the manufacturing teams in scheduling, problem solving, product quality, employee relations and process improvements to meet the company’s goals and objectives.在時間管理，問題解決，產品質量，員工關系，以及流程改進等方面支持生產團隊工作，以滿足公司目標和期望9.Ensure that all personnel perform in a safe manner and that an accident free environment is maintained.確保所有個人以安全行為進行運作，以及維持一個無事故的生產環(huán)境。10.Develop and monitor appropriate training, training documentation, training policies and training procedures consistent with company and regulatory guidelines.開發(fā)和監(jiān)督適當的符合公司法規(guī)指南的培訓，培訓文件，培訓政策以及培訓程序，11.Administer proper floor scheduling to meet master scheduling of product.管理適當的流程計劃，以滿足公司的產品生產計劃12.Provide leadership essential to drive continuous improvement in manufacturing.提供不可缺少的領導力，在生產部促使持續(xù)的改善13.Direct the organization in a manner in which facilities, procedures, product and employee work practices meet the requirements of ISO and FDA regulatory statutes.以適當方式指導組織在設施，程序，產品和員工工作行為方面來滿足ISO和FDA法規(guī)要求14.Authorized to identify and initiate corrective action of non-conformance in documentation, design, equipment, facilities, and processes including those activities covered by the Quality System.在文件體系，設計，設備，設施以及流程等方面包括其活動均被質量體系所覆蓋，授權他人以界定和啟動不合格項的糾正措施15.Drive and adopt 6-Sigma, Validation and Lean manufacturing concept to continuously improve the productivities and quality.驅動和采納6-Sigma，驗證和精益生產概念，以持續(xù)改進生產力和質量16.Performs other duties as may be required by supervisor.按照上級主管要求，管理其它職責17.Support micro-lab on new sterilization process validation and sterilization process re-validation.支持微生物部門在新滅菌過程驗證和滅菌過程的重新驗證的工作SKILLS AND ABILITIES（技能）1.BS/BA in Business or Engineering is preferred, relevant working experience.在商務或者工程擁有工學碩士最好，以及相關工作經驗2.Have relevant manufacturing management experience in the medical device field, more than 6 years’ working experience.具備在醫(yī)療器械領域相關制造管理經驗，超過6年的工作經歷3.Good command of both spoken and written Chinese and English能夠在書寫和口頭交流駕馭中文和英文4.Sufficient software application proficiency in MS office.在微軟辦公軟件方面熟練應用5.Extensive manufacturing knowledge including but not limited to inventory/work-in-process principles, labor efficiencies, yield tracking, production scheduling/planning.開闊的生產知識包括但不僅限于庫存、工作流程原理，勞動力效率，產出以及生產時間和計劃6.Financial knowledge includes but not limited to budgets, standard costing, variance analysis, fixed and variable costing.財務知識包括但不僅限于預算，標準成本，差異分析，固定和變動成本分析7.Ability to work in a high stress, high productivity and rapidly changing environment.具備在高壓力，高效率和快速改變的環(huán)境先工作的能力8.Ability to be a self-starter who identifies, resolves, and reports on issues in timely and effective manner.具備自我激勵能力，能夠及時和有效率的確定，解決和報告能力

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