Technical Author
医科达(上海)软件研发中心
- 公司规模:50-150人
- 公司性质:外资(欧美)
- 公司行业:计算机软件
职位信息
- 发布日期:2013-09-05
- 工作地点:北京-昌平区
- 招聘人数:若干
- 工作经验:二年以上
- 学历要求:大专
- 职位类别:文档工程师
职位描述
Job Description
? Develop User & Technical Service manuals as part of new product development.
在新产品开发过程中编制用户及技术维修手册
? Maintain and update existing User & Technical Service manuals.
维护并更新已有用户及技术维修手册
? Collect and process relevant information from medical and engineering specialists.
从医学和工程专家处收集并处理相关信息
? Working as an individual as well as part of a team.
能够独立工作,同时具有较强的团队合作精神
? Provide input and shape documentation strategy, e.g. emedia, epublishing and other information delivery methods.
提供输入和形成文件的策略,如:电子媒体,电子出版和其他信息传递方法
? Adhere to processes, company templates and standards.
坚持流程,公司模板和标准
? Plan, manage and report document progress.
计划、管理和汇报文档进展
? Produce documentation plans, review forms and device master files ensuring compliance with audit criteria.
制定文档计划,评估表以及保有主文档确保与稽核标准相符
? Assemble documents into PDF format; working with suppliers for quality checking and preparing for delivery.
将文档转换成PDF格式;与供应商协作进行质量检查及发运准备
Responsibilities
? To work within existing documentation processes and to company standards.
根据已有的文档流程和公司标准工作
? To proactively obtain and collate design information as source material for the creation of required documentation.
预先收集、比较设计信息,据此产生所需文档
? To work within cross-functional design project teams, defining documentation and information requirements.
在交叉功能的设计团队内工作,定义所需文档和信息
? To work with Quality Assurance, Regulatory Affairs and Safety departments to make sure documents are compliant.
与质量保证、法规事务和安全部门协作,确保文档合乎规范
? To participate in project and other meetings as required making sure that the needs of documentation activities are considered and distribute relevant information throughout the department and to customers.
根据需要参加项目和其他会议,确保考虑产生文档所需信息并将相关信息传达至部门和客户
? To plan and manage documentation creation progress, to report any risks or slippage to project team / functional management.
计划和管理文档创建流程,向项目团队/主管经理报告文档创建的风险或质量下降
? To proactively ensure that document review process and schedules are met.
主动确保符合文档评估流程和进度
? That First-of-Kind meets necessary quality standards.
符合必须的质量标准
Relevant knowledge, skills and competencies
? Recognized scientific or engineering qualification.
认可的科学或工程资质
? A degree in a relevant engineering discipline
相关工科学历背景
? Documented business/industrial experience.
商务/工业领域工作经验
? Excellent communication skills, both verbal and written.
优良的口头和书面沟通技巧
? Demonstrate initiative.
有上进心
? Ability to plan and control project progress.
能够计划和控制项目进程
? Strong interpersonal skills.
优良的人际技巧
? Prepared to learn new skills.
乐于学习新的知识/技巧
? Prepared to undertake international travel.
可以根据需要出差
? Develop User & Technical Service manuals as part of new product development.
在新产品开发过程中编制用户及技术维修手册
? Maintain and update existing User & Technical Service manuals.
维护并更新已有用户及技术维修手册
? Collect and process relevant information from medical and engineering specialists.
从医学和工程专家处收集并处理相关信息
? Working as an individual as well as part of a team.
能够独立工作,同时具有较强的团队合作精神
? Provide input and shape documentation strategy, e.g. emedia, epublishing and other information delivery methods.
提供输入和形成文件的策略,如:电子媒体,电子出版和其他信息传递方法
? Adhere to processes, company templates and standards.
坚持流程,公司模板和标准
? Plan, manage and report document progress.
计划、管理和汇报文档进展
? Produce documentation plans, review forms and device master files ensuring compliance with audit criteria.
制定文档计划,评估表以及保有主文档确保与稽核标准相符
? Assemble documents into PDF format; working with suppliers for quality checking and preparing for delivery.
将文档转换成PDF格式;与供应商协作进行质量检查及发运准备
Responsibilities
? To work within existing documentation processes and to company standards.
根据已有的文档流程和公司标准工作
? To proactively obtain and collate design information as source material for the creation of required documentation.
预先收集、比较设计信息,据此产生所需文档
? To work within cross-functional design project teams, defining documentation and information requirements.
在交叉功能的设计团队内工作,定义所需文档和信息
? To work with Quality Assurance, Regulatory Affairs and Safety departments to make sure documents are compliant.
与质量保证、法规事务和安全部门协作,确保文档合乎规范
? To participate in project and other meetings as required making sure that the needs of documentation activities are considered and distribute relevant information throughout the department and to customers.
根据需要参加项目和其他会议,确保考虑产生文档所需信息并将相关信息传达至部门和客户
? To plan and manage documentation creation progress, to report any risks or slippage to project team / functional management.
计划和管理文档创建流程,向项目团队/主管经理报告文档创建的风险或质量下降
? To proactively ensure that document review process and schedules are met.
主动确保符合文档评估流程和进度
? That First-of-Kind meets necessary quality standards.
符合必须的质量标准
Relevant knowledge, skills and competencies
? Recognized scientific or engineering qualification.
认可的科学或工程资质
? A degree in a relevant engineering discipline
相关工科学历背景
? Documented business/industrial experience.
商务/工业领域工作经验
? Excellent communication skills, both verbal and written.
优良的口头和书面沟通技巧
? Demonstrate initiative.
有上进心
? Ability to plan and control project progress.
能够计划和控制项目进程
? Strong interpersonal skills.
优良的人际技巧
? Prepared to learn new skills.
乐于学习新的知识/技巧
? Prepared to undertake international travel.
可以根据需要出差
公司介绍
Elekta is a human care company pioneering significant innovations and clinical solutions for treating cancer and brain disorders.
Elekta is a high technology medical device company working with the latest technology and tools within the development of software, electronics and hardware. Our manufacturing site has recently seen major investment in the latest tools and processes required to provide an efficient manufacturing process.
Elekta was founded in 1972 by the late Lars Leksell, Professor of Neurosurgery at the Karolinska Institute in Stockholm, Sweden. Today, Elekta solutions in oncology and neurosurgery are used in over 5,000 hospitals globally, and every day more than 100,000 patients receive diagnosis, treatment or follow-up with the help of a solution from the Elekta Group.
Elekta employs around 2,500 employees globally. The corporate headquarter is located in Stockholm, Sweden, and the company is listed on the Nordic Exchange under the ticker EKTAB.
Elekta has two legal entities, one JV, and one branch organization in China with functions of R&D, Engineering, Manufacturing, Purchasing, QA/RA, and other support functions.
Legal Entities: Elekta (Shanghai) Instruments Ltd, located in Shanghai and Beijing; Shanghai Elekta Oncology Systems Ltd, located in Shanghai
Joint Venture: Elekta BMEI (Beijing) Medical Equipment Co. Ltd, located in Beijing
Branch organization: CMS Worldwide Corp. Shanghai Rep. Office, located in Shanghai. CMS is the software development division responsible for software development around the world within the Elekta Groups
Elekta’s culture values diversity. By combining different traditions and backgrounds of all our employees we can create a positive and flexible organization.
We provide the opportunity and support to enable individuals to use their competencies to develop within a global environment.
Join us, by working together we can fight serious disease and enhance quality of life.
医科达 AB (公众)公司在华独资及合资企业
医科达 AB (公众)公司是跨国性医疗技术集团,总部设在瑞典斯德哥尔摩,并在斯德哥尔摩证交所上市。医科达 AB (公众) 公司是 医科达北研(北京)医疗器械有限公司、医科达上海软件研发中心(美国希迈仕国际公司上海代表处)、医科达(上海)医疗器械有限公司、以及上海医科达放疗设备有限公司的母公司。
医科达 AB (公众)公司在华独资及合资企业主要经营放疗和神经外科两大类产品,包括直线加速器及其相关附属产品,致力于建立本地化的研发、生产和技术支持,为客户提供更完善的服务。我们在此虚位以待,邀您共创中国放疗和神经外科的未来。
公司地址
北京:北京市昌平科技园区创新路21号,
上海:上海市浦东新区世纪大道1528号 陆家嘴基金大厦5F、3F 301, 上海市浦东新区金海路1000号B1
Elekta is a high technology medical device company working with the latest technology and tools within the development of software, electronics and hardware. Our manufacturing site has recently seen major investment in the latest tools and processes required to provide an efficient manufacturing process.
Elekta was founded in 1972 by the late Lars Leksell, Professor of Neurosurgery at the Karolinska Institute in Stockholm, Sweden. Today, Elekta solutions in oncology and neurosurgery are used in over 5,000 hospitals globally, and every day more than 100,000 patients receive diagnosis, treatment or follow-up with the help of a solution from the Elekta Group.
Elekta employs around 2,500 employees globally. The corporate headquarter is located in Stockholm, Sweden, and the company is listed on the Nordic Exchange under the ticker EKTAB.
Elekta has two legal entities, one JV, and one branch organization in China with functions of R&D, Engineering, Manufacturing, Purchasing, QA/RA, and other support functions.
Legal Entities: Elekta (Shanghai) Instruments Ltd, located in Shanghai and Beijing; Shanghai Elekta Oncology Systems Ltd, located in Shanghai
Joint Venture: Elekta BMEI (Beijing) Medical Equipment Co. Ltd, located in Beijing
Branch organization: CMS Worldwide Corp. Shanghai Rep. Office, located in Shanghai. CMS is the software development division responsible for software development around the world within the Elekta Groups
Elekta’s culture values diversity. By combining different traditions and backgrounds of all our employees we can create a positive and flexible organization.
We provide the opportunity and support to enable individuals to use their competencies to develop within a global environment.
Join us, by working together we can fight serious disease and enhance quality of life.
医科达 AB (公众)公司在华独资及合资企业
医科达 AB (公众)公司是跨国性医疗技术集团,总部设在瑞典斯德哥尔摩,并在斯德哥尔摩证交所上市。医科达 AB (公众) 公司是 医科达北研(北京)医疗器械有限公司、医科达上海软件研发中心(美国希迈仕国际公司上海代表处)、医科达(上海)医疗器械有限公司、以及上海医科达放疗设备有限公司的母公司。
医科达 AB (公众)公司在华独资及合资企业主要经营放疗和神经外科两大类产品,包括直线加速器及其相关附属产品,致力于建立本地化的研发、生产和技术支持,为客户提供更完善的服务。我们在此虚位以待,邀您共创中国放疗和神经外科的未来。
公司地址
北京:北京市昌平科技园区创新路21号,
上海:上海市浦东新区世纪大道1528号 陆家嘴基金大厦5F、3F 301, 上海市浦东新区金海路1000号B1
联系方式
- 公司网站:http://www.elekta.com
- 公司地址:上海市浦东新区世纪大道1528号 陆家嘴基金大厦5F、3F 301
- 邮政编码:200122