沈阳市 铁西区 Tasks By the development of chinese green manufacturing system, and more focus from BMW AG, the energy efficiency and energy mgt. compliance are playing more and more important role. In order to fulfill serise deep and compehrensive requirments in energy mgt. audit and supervision, align reform of energy markting and emission policy by government and BMW AG: The laws and regulations to be observed and implemented. Coorperation and communication with government to be reinforced. Internal ...

MAIN REPONSIBILITIES / DUTIES Maximize the value of Pfizer products to Chinese patients and health care professional through medical activities in regional level. Establish, build and manage relationship with KOLs. Implement medical/research/disease management programs. Introduce new concept through medical education to help doctors to improve patients’ outcome. Conduct medical to medical communication to transport product knowledge and therapeutic update to key influencers and stakeholders. Pro...

1. The preparation and execution of the international regulatory affairs departments intelligence strategy. Led the implementation of regulatory intelligence ensuring strategy is aligned to the business needs; 2. Develop and implement systems for monitoring, analyzing and communicating international regulatory intelligence; 3. Monitor and analyze the external regulatory environment, including guidance and regulations from regulatory authorities, trade organizations, working groups, and relevant ...

岗位描述： 对分析检验、质量研究、稳定性研究、部分申报资料撰写等工作负责； 能够带领团队，并兼顾每个人的工作情况，按时分配任务并及时检查完成情况； 负责承担部门管理制度文件管理与监督执行 ； 协助研发分析中心负责人进行实验室管理； 对其他分析人员的分析工作（检测数据、图谱、原始记录）进行专业复核，及时发现分析工作中出现的问题及异常情况，并汇报上级领导； 负责对小组内研发、申报、转生产中质量研究、质量标准、稳定性研究、申报资料等工作进行审核、指导工作。 任职资格： 大学本科及以上学历，药物分析、分析化学、药学、化学及相关专业； 有5年以上药物分析工作经验； 具有较高的药物分析理论知识和操作技能，熟练操作常用药物检测设备； 熟悉Ch.P.、USP、EP，熟悉药品研发流程、政策法规及相关技术要求； 熟悉药品注册申报中质量研究、质量标准起草和稳定性研究的资料编写，了解国内外药物分析新技术发展方向； 了解生产管理、质量管理等方面知识。 职能类别： 化学分析测试员 关键字： 高级研究员 化药分析 药品分析 微信分享 联系方式 上班地址：北京市北京经济技术开发区景园北街2号38-1...

1. Develop and implement registration plan for new products in oversea markets within relevant therapeutic areas. 2. Independently prepare registration documents for submission, ensure the quality, accuracy and format of regulatory submissions and other documentation comply with applicable laws, regulations, and company standards. 3. Manage registration submissions for new products registration and clinical trial applications. 4. Manage registration submissions for license renewal and variations...

蓬莱市 Position Title: Quantity Surveyor Lead Location: Penglai, Shandong, China Duration: 2 years contract Start date: Apr. 2019 Job Purpose: Quantity Surveyors primary responsibility is to manage the re-measurable portion of the project contract price and cost, from interim re-measurements through to final accounts close-out and in accordance with established company policies and project procedures, reporting directly to the Commercial Manager. Assist the Commercial Manager to guide and lead the ...

SUMMARY: ？ Operates from a deep understanding of the total situation. Collaborates with other caregivers to challenge and coordinate institutional resources to maximize advocacy for patient and family care in achieving the most effective outcomes for postpartum patient and other cross-cover need. ESSENTIAL TASKS: ？ Assess, plan, implement and evaluate the nursing care to newborns by applying general accepted standards of practice. ？ Deliver safe and competent nursing care to newborns as well as ...

平均月入$13,000 - $16,000 負責包裝、點核、運送航餐及航機用品 無須經驗、學歷要求；需涉及體力勞動工作...

平均月入$18,000 - $21,000 (自動化機械/冷凍/樓宇設備) 負責保養及維修工作 具三年相關工作經驗 (少於三年者可考慮為見習工程技術員)...

平均月入$13,000 負責貨倉內的交收、倉務及採購事宜 無須經驗、學歷要求；需涉及體力勞動工作...

平均月入$20,800 - $24,000 負責點核、運送、搬運航餐及航機用品 持18或19號駕駛執照...

平均月入$15,600 - $17,000 負責與機艙服務員聯絡、核對航餐及航機用品之數量 持專上學院文憑或以上學歷...

上海市 招聘类型：社招 工作性质：全职 职位描述 1) First level support for all IT issue. 2) Ensures close cooperation between internal IT team and external IT service providers. 3) Operationally manage assets (SW and HW) throughout the entire asset life cycle. 4) Ensure that End user system incident tickets are addressed to agreed service levels through prioritization, incident recording, recognition, isolation, resolution and follow up. 5) Analyzes IT incident trend and provide preventive action to avoid repetitive i...

工作职责: This position is the Corporate Quality Authority for the supplier management. Provides strategic quality programs to Edding Pharma(EDP) manufacture sites to ensure that supplier management procedures, regulatory quality and compliance standards and guidance are implemented and are sustainable, audit/evaluate and approved supplier accordingly. Monitors quality and compliance activities in suppliers to ensure that all quality activities operations are in compliance with cGMP’s, Regulatory st...

上海市 Job Description Position: Office Administrator Exciting opportunity for the right candidate to participate in building from the start-up phase a new clinical stage neurology focused biotech company in China, developing CNS drugs for the China and other Asia markets Benefit from strong support system of parent US company Location: Shanghai, China Reporting Line: GM of BioShin Job Purpose: At BioShin, our success depends on our people, productivity, and procedures. An office administrator is t...

上海市 浦东新区 Responsibilities: 1. Analyze pharmacokinetic data using noncompartmental analysis, ensure quality and timely delivery of the project PK deliverables to Frontage clients. Assist with the implementation of quality control (QC) assessment and procedures, as well as scientific review. 使用非房室模型分析PK数据，确保PK项目能保质保量的按时交付给客户。协助实施QC评估和流程，以及技术审阅。 2. Write bioequivalence report independently with proficiency and contribute to other clinical pharmacology report for regulatory submission. 能够独立撰写生物等效性报告...

Clinical Research Associate performs site management, site administration and site monitoring responsibility for clinical studies according to Covance Standard Operating Procedures, ICH Guidelines and GCP, including pre-study qualification and initiation visits, routine monitoring, close-out of clinical sites, and maintenance of study files. Responsibilities and duties include, but are not limited to the following: ?Take charge of all aspects of Site Management as prescribed in the project plans...

中国 This position is for Covance FSPx BU. CRA Trainee will be outsourced to global pharma after 8-10 weeks CRA training program. Requirement: Bachelor degree (or equivalent) or above in medical, pharmaceutical, etc. 6 – 12 months CRA experience (up to 18 months), prefer global experience Other experience in clinical development industry such as CRC, Project Assistant, etc also counts Good communication skills Fluent English both spoken and written Anti-pressure and prefer extrovert personality Lo...

北京市 朝阳区 This position is for Covance FSPx BU. CRA Trainee will be outsourced to global pharma after 8-10 weeks CRA training program. Requirement: Bachelor degree (or equivalent) or above in medical, pharmaceutical, etc. 6 – 12 months CRA experience (up to 18 months), prefer global experience Other experience in clinical development industry such as CRC, Project Assistant, etc also counts Good communication skills Fluent English both spoken and written Anti-pressure and prefer extrovert personali...

上海市 浦东新区 主要职责Main Responsibilities 新设备的安装、调试； New machine installation and commissioning. 根据客户需求，提供故障分析、问题解决、零件更换以及日常维修和紧急服务。 Service including problem analysis, troubleshooting, repair, replace parts, daily maintenance and emergency service required by customer and etc. 提供预防性维护以及设备检查 Preventive maintenance and inspection 生产支持和培训 Production assistant & training for customer. 根据服务内容创建服务报告，评估设备状态 Create service reports with essential content, estimate machine conditions 提供售前售后技术支持，以及备件销售 Provi...