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生产经理S3

苏州碧迪医疗器械有限公司

苏州

  • 工作年限无要求
  • 学历要求无要求
  • 招聘人数
  • 发布日期01-18 发布
  • 语言要求
职位信息

职位名称： 生产经理S3

类别名称：

职位描述：
KEY RESPONSIBILITIES（主要职责）1.Supervises employees in the area day-to-day manufacturing operations.日常管理生产运作的所有生产员工2.Responsible for hiring (with HR input), training, performance evaluation and discipline of employees supervised.负责招聘（与HR合作），培训，业绩考核以及监管所有生产员工的纪律3.Maintains a variety of production records and documents to reflect schedules, performance and procedures.维护多种的生产记录和文件，以适应时间，业绩和程序的改变4.Generates effective communications, good relations, and a positive image with inside customers, suppliers and coworkers, promoting courtesy, objectivity, fairness and teamwork.具备有效的沟通，良好的关系，与内部顾客，供应商以及合作方打交道，保持谦恭有礼，明确目标，公平和团队合作形象5.Ensure that accurate and complete records of department activities are kept, and that they meet regulatory requirements.确认准确和完整的部门工作记录，并保留记录。所有记录符合法务要求6.Develop and monitor production schedules, staffing requirements and budgets. Manage implementation of new processes; technologies, or tolling needed to manufacture products.发展和监管生产时间，与员工发展要求以及预算。管理好新的流程，技术和生产消耗7.Facilitate a team based manufacturing environment按照生产环境需求发展生产团队8.Support the manufacturing teams in scheduling, problem solving, product quality, employee relations and process improvements to meet the company’s goals and objectives.在时间管理，问题解决，产品质量，员工关系，以及流程改进等方面支持生产团队工作，以满足公司目标和期望9.Ensure that all personnel perform in a safe manner and that an accident free environment is maintained.确保所有个人以安全行为进行运作，以及维持一个无事故的生产环境。10.Develop and monitor appropriate training, training documentation, training policies and training procedures consistent with company and regulatory guidelines.开发和监督适当的符合公司法规指南的培训，培训文件，培训政策以及培训程序，11.Administer proper floor scheduling to meet master scheduling of product.管理适当的流程计划，以满足公司的产品生产计划12.Provide leadership essential to drive continuous improvement in manufacturing.提供不可缺少的领导力，在生产部促使持续的改善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.以适当方式指导组织在设施，程序，产品和员工工作行为方面来满足ISO和FDA法规要求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.在文件体系，设计，设备，设施以及流程等方面包括其活动均被质量体系所覆盖，授权他人以界定和启动不合格项的纠正措施15.Drive and adopt 6-Sigma, Validation and Lean manufacturing concept to continuously improve the productivities and quality.驱动和采纳6-Sigma，验证和精益生产概念，以持续改进生产力和质量16.Performs other duties as may be required by supervisor.按照上级主管要求，管理其它职责17.Support micro-lab on new sterilization process validation and sterilization process re-validation.支持微生物部门在新灭菌过程验证和灭菌过程的重新验证的工作SKILLS AND ABILITIES（技能）1.BS/BA in Business or Engineering is preferred, relevant working experience.在商务或者工程拥有工学硕士最好，以及相关工作经验2.Have relevant manufacturing management experience in the medical device field, more than 6 years’ working experience.具备在医疗器械领域相关制造管理经验，超过6年的工作经历3.Good command of both spoken and written Chinese and English能够在书写和口头交流驾驭中文和英文4.Sufficient software application proficiency in MS office.在微软办公软件方面熟练应用5.Extensive manufacturing knowledge including but not limited to inventory/work-in-process principles, labor efficiencies, yield tracking, production scheduling/planning.开阔的生产知识包括但不仅限于库存、工作流程原理，劳动力效率，产出以及生产时间和计划6.Financial knowledge includes but not limited to budgets, standard costing, variance analysis, fixed and variable costing.财务知识包括但不仅限于预算，标准成本，差异分析，固定和变动成本分析7.Ability to work in a high stress, high productivity and rapidly changing environment.具备在高压力，高效率和快速改变的环境先工作的能力8.Ability to be a self-starter who identifies, resolves, and reports on issues in timely and effective manner.具备自我激励能力，能够及时和有效率的确定，解决和报告能力
任职要求：
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