IT Manager, Regulatory & Safety
职位描述
职位描述:
? Janssen R&D Information Technology is recruiting an IT Manager, Janssen R&D, Regulatory and Safety. This position can be located in Shanghai, China or Beijing, China.
? This position will deliver against Janssen R&D China and Enterprise business strategy as we build, advance and deliver on our pipeline through the strategic use of information technology in Regulatory and Safety. This position will be dotted line and closely aligned with the Global Janssen R&D Regulatory and Safety Team.
? The role represents expertise in the organization in the discipline of project, program and portfolio management. Roles in this sub-function are accountable for achieving project objectives, ensuring effective integration of new systems and technologies, meeting time and budget requirements, directing all project resources, and helping the business partner(s) realize the desired business goals for the project(s).This role will assume responsibility and direct accountability for the delivery of various components essential for the success of Regulatory and Safety information management within Janssen R&D China. In addition, this role will have cross-sector responsibility as we drive the OneChina Strategy. These components include the Product & Lifecycle Registration System, the Submission Planning, Tracking, and Processing utilities, as well as the future state Document Management System. The incumbent will be expected to possess a clear understanding of integrated, platform technology and work closely with external service providers to ensure delivery of solutions.
? Responsibilities include: Possesses a clear grasp of current Regulatory and Safety trends in information management and has a perspective on the future direction of the industry through relationships with vendors, industry peers, and internal business partners and stakeholders; Leads large, moderate to complex projects, programs, or initiatives across the franchise or enterprise (central, regional, and local affiliates, as well as cross-sector), including a GxP environment; Builds and manages strong relationships across all IT, legal, finance, and the impacted Business IT areas, etc.; Works effectively as part of a team; Operates effectively in a global environment; Solves complex or unusual problems in consideration of the potential impacts; Negotiates the needs of multiple users or business partners and can adapt to organizational and system complexity and ambiguity; Provides an effective balance between IT standards and strategies and business needs to guide well-informed decisions; Applies compliance requirements within scope of responsibility, provides documentation as necessary, and participates in compliance activities as required.
? Knowledge for this position should include: Deep understanding of current Regulatory and Safety technologies and processes associated with conducting regulatory specific activities; In-depth knowledge of all areas of IT and the resources available to deliver projects, programs or manage portfolios; Strong understanding of the current and future state technology and applications within the Regulatory Information Management (RIM) platform; Advanced knowledge of the strategic plans/initiatives of the Global Regulatory Affairs and Safety functions or work process area; Knowledge within the Master Data Management (MDM) domain and understanding the importance and framework of effective data governance and stewardship; Understanding of industry defined data standards and associated formats (i.e. EVMPD, IDMP, eCTD, etc.); Understanding of industry defined data standards and associated formats supporting the Adverse Event processing and reporting workflow for electronic transmission of individual safety reports (ICSR and E2B). Understanding of the business impact of different solutions, and the ability to assess and communicate the tradeoffs between business needs, technology requirements, costs, and risk; Understanding of departmental budgets and the ability to allocate resources accordingly; Understanding of the company’s strategic vision and future products, services, and strategies globally; Ability to identify and recover any troubled projects, programs and/or streamline a portfolio.
? Supervision Received/Provided: Functions very independently, receiving high-level and/or strategic guidance; able to self-direct, plan and execute initiatives (projects, programs, strategies); Manages business partner expectations at a senior level, resolving conflicts between requirements and budgets; Works independently in formulating innovative ideas and solutions on products, processes, and systems; Provides leadership, mentorship, or guidance to others; Manage vendors necessary to complete a project.
企业简介
美国强生公司创建于1886年,目前在全球60个国家建立了250多家分公司,是目前世界上最具综合性、业务分布范围最广的卫生保健产品的制造商和相关服务提供商,业务领域主要包括制药,医疗器械和消费品。
西安杨森制药有限公司是美国强生公司在华最大的子公司,成立于1985年。公司管理中心在北京,生产基地位于西安,在全国28个城市设有办事处,在华员工超过3000人。在过去的25年中,西安杨森保持持续稳定发展,成为了中国领先的合资制药企业。
西安杨森不断引进和生产多种创新的、高品质的药品,其产品包括多种高质量的处方药,以及广受患者信赖的非处方药物。西安杨森依托强生公司全球强大的研究开发体系,着眼于未来,不断引进新的药品,计划上市生物制剂、肿瘤、心血管、风湿和泌尿等更多领域的产品以服务于中国的广大患者。
西安杨森公司遵从强生信条的原则,致力于公司的长期发展。这是公司在过去取得成功的基石,也是未来成长的保障。
西安杨森公司获得众多奖项和赞誉,比如《财富》杂志评选的“中国最受赞赏的外资企业”及“人力资源经理眼中的热门雇主”;中国中央电视台 “2005CCTV中国年度雇主”;CRF评选的2007-2008年度北京地区“中国杰出雇主”;2008年与强生在华公司一起荣获“第六届中国大学生最佳雇主奖和进步飞速奖”称号,和2009年“第七届中国大学生最佳雇主奖”,并位列医药行业第一名。2010年强生在华公司荣获“第八届中国大学生最佳雇主制药/医疗行业最佳雇主第一名”。这是继上届强生公司获得医药行业第一名后再次蝉联这项荣誉。
热门区域招聘: 重庆 北京 上海 浙江 江苏 广东 山东 湖南 安徽 河北
上海招聘企业: 百进冠合(海南) 医疗科技有限公司 上海华茂药业有限公司 上海信谊药厂有限公司 上海强生制药 欧姆龙健康医疗(中国)有限公司 青海瑞成药业(集团)有限公司 上海交通大学医学院附属瑞金医院 复旦大学附属中山医院 上海复星医药 上海医药集团
职位发布日期: 2016-11-23