Regulatory Affairs assistant manager 飞利浦（中国）投资有限公司 Philips (China) Investment Co.,Ltd. 北京 2-2.5万/月 10-18

学历要求：本科|工作经验：5-7年|公司性质：外资（欧美）|公司规模：10000人以上

Your challenge Government relations: Familiar with the officials and understanding their requirements for timely approvals.Regulations: In depth-understanding and application of SFDA and CQC regulations and the related regulatory process. Technical expertise: Knowledge of process and methods and medical product area such as product specifications, product developments / expansions and product safety. Understanding of the IEC and related GB standard for good communications with the BIU and CFDA or CQC testing lab’s engineers.Excellent communications skill with internal and external customers. Duties and responsibilities include: Advise internal stakeholders (marketing, manufacturing, R&D, etc.) regarding current/pending guidance, regulations, Agency/industry initiatives, etc. Create detailed written regulatory plans that can be used to target domestic and international shipment dates.Develop and take the ownership of China CFDA submissions Support Key market RA team on global registrations Establish active communications with regulatory agencies in China. Review and approve advertising, promotional items and labeling for regulatory complianceIdentify potential regulatory approvals risks based on changes in regulations, standards country specific issues or other unique characteristics of the project.Communicate application progress to internal stakeholdersCollaborate with worldwide colleagues regarding license renewals and updatesMaintain regulatory files and tracking databases as required Requirements: BS in engineering discipline or equivalent education, experience, training.At least 5 years regulatory experience in medical device industry.Experience in China local manufactured or local developed products will be a plus. Strong understanding of China FDA and other major international regulationsBe able to manage multiple tasks and perform with accuracy and a high attention to detail Requires strong written, oral and interpersonal skills to be able to effectively compose agency submissions, interface interdepartmentally and complete assignments with minimal supervision. Proficient in English communication including reading, writing, speaking and listening. Travel frequency: 25-30%

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Tendering specialist（投标专员） 泰科电子（上海）有限公司 上海-徐汇区 0.8-1万/月 10-18

学历要求：|工作经验：3-4年|公司性质：外资（欧美）|公司规模：10000人以上

Overview As a key person of tender function, to coordinate and drive centralized biddings under regional PSBs, establish tracking record within Utility system, and implement bidding process improvement. Responsibilities - Coordinate and drive centralized biddings under regional PSBs, establish tracking record within Utility system. - Handle direct bidding project including legal process, financial process and document preparation. - Implement bidding process improvement - Assist with research and analysis for competition and price for South Grid and State Grid centralized bidding. - Support distributors tender by TE qualification document supply and tender training if in need. Qualification 1. College degree or above. 2. More than 6 years working experience, and at least 3 years’ experience in tendering, relevant experience in Utility is preferable. 3. Good English communication skills, orally and in writing. 4. Good at MS Office softwares (Word, Excel, PowerPoint). 5. Proactive and willing to learn.

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医药信息专员-厦门-麻醉（特药） 默沙东（中国）投资有限公司 厦门 10-18

学历要求：大专|工作经验：2年|公司性质：外资（欧美）|公司规模：

医院销售代表 直线上级: 地区经理 职责描述:1. 区域销售计划执行和专业教育推广根据区域实际情况，制定并执行销售计划发展及实现产品的有效的医院覆盖，确保完成销售目标负责相关医院的专业教育活动的开展，协助跨区域的专业教育培训活动2.重点客户的管理建立和维护与重点客户和设备科科长良好的合作关系以促进业务的持续增长发展与KOL的良好沟通，开拓大客户业务，有效传播公司的品牌与专业教育理念职位要求:大学专科及以上学历，医药或护理相关专业优先一年以上医药及相关行业销售经验或有医护人员,医生/护士从业经验者愿意在应聘区域工作并长期发展具有独立开展业务的能力和学习能力良好的职业操守和沟通技巧勤奋,坚韧,乐观,积极向上

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Medical Communication Officer 拜耳医药保健有限公司 北京 1-1.8万/月 10-18

学历要求：本科|工作经验：3-4年|公司性质：合资|公司规模：500-1000人

Develop product knowledge across the Bayer Healthcare (BHC) Pharmaceuticals, Consumer Care (CC) and Medical Care (MC) products, and in particular responsible products and therapeutic area. Answer medical questions from doctors as well as escalated queries from medical hotline. By providing well-balanced, high-quality and most up-to-date information to ensure appropriate usage of Bayer products. Proactively accelerate medical material generation which includes FAQ, standard response letter, and non-promotional material, such as MC newsletter and external newsletter. Facilitate internal scientific communication to improve competence of both medical representatives and district managers. Support TL engagement with timely information update on disease and clinical practice. Lead the role as information expert and facilitate related training to internal & external customers if needed. Proactively figure out innovative ways in facilitating scientific communication with both internal and external customers Provide technical guidance and support to Junior MCO/MCO to fulfil their tasks. Who You Are Education: Bachelor degree or above, major in medical information is preferred Skills: Good communication skill, Eager to face challenges Self-learning ability, problem solving Experience: More than 3 year experience in MNC medical information function Personal characters: honesty, integrity

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实习医药代表-江门 北京诺华制药有限公司 Beijing Novartis Pharma Co., Ltd 江门 2-3千/月 10-18

学历要求：|工作经验：|公司性质：外资（欧美）|公司规模：500-1000人

【扬帆成长计划简介】2005年起诺华推出了针对毕业新人发展的"扬帆成长计划"。"扬帆成长计划"为高速发展的公司业务储备了大批优秀的人才，更为有志成为诺华员工的优秀应届毕业生提供了学习和实践的良机，帮助他们为即将开始的职业生涯做足准备。表现优异的实习生将有机会成为诺华的正式员工，助你在职业旅途上扬帆启航。主要职责：1.通过一系列培训，并跟随导师参加医院拜访和组织学术推广活动，了解诺华的企业文化和核心价值观，掌握相关医学知识、产品知识，了解如何宣传和推广公司产品、及时准确反馈市场信息，熟悉诺华医药代表的角色和专业销售的一般过程及技巧;2.每项培训结束以及全部实习结束时，接受学习成果的考核;3.实习期间不承担销售指标。任职条件1.2019届毕业生，专科及以上学历，医药相关专业；2.良好的沟通能力及人际敏感度；3.较强的快速学习能力；4.乐观积极，乐于接受挑战；5.良好的团队合作精神。

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Lead - Regulatory Affairs 3179589 GE医疗集团 北京 10-18

学历要求：本科|工作经验：3-4年|公司性质：外资（欧美）|公司规模：少于50人

Essential Responsibilities 1. Provides regulatory input for product development to ensure compliance to regulatory requirements for target markets 2. Develops regulatory strategies to help guide regulatory submission pathways, taking into consideration regulatory requirements (including product testing, clinical data, etc), product claims and country regulatory dependencies to ensure optimized sequencing for submissions, 3. Works with a cross functional team to prepare and submit regulatory submissions to regulatory authorities for the purpose of obtaining authorization for market launch. 4. Assesses changes in existing products to and determines the need for new / revised licenses or registrations. 5. Develops plan for timely submission of renewal registrations for applicable countries per business plan, to ensure continued product supply in those countries. 6. Reviews and approves advertising and promotion material to ensure consistency with approved claims and regulatory requirements. 7. Contributes to writing and editing technical documents 8. Researches, analyzes, integrates and organizes background information from diverse sources for regulatory submissions 9. Understands and applies regulatory requirements and their impacts for submissions 11. Ensures compliance with pre- and post-market product approval requirements 10. Supports regulatory inspections as required. 11. Assesses adverse events and field actions for reportability to regulatory authorities and prepares and submits reportable events and recalls in a timely manner to regulatory authorities, as per country regulations. 12. Performs a broad variety of tasks in support of product and process design as assigned by the departmental manager Role Summary/Purpose This position provides subject matter guidance. He/she works within a team of Regulatory Affairs professionals to ensure GEHC establishes best practices in compliance with regulatory requirements. The Regulatory Affairs Leader will be involved with regulatory activities in the areas such as premarket submissions, post-market reporting, regulatory intelligence, regulatory requirements flow-down advertising and promotion review, product labeling compliance, etc., Qualifications/Requirements • Bachelor's Degree or a minimum of 4 years work experience. • Minimum of 1 year experience working in a regulated industry • Where required by law the Technical Responsible will meet required qualifications in terms of education, certifications and experience (for example, Pharmacist in Brazil). • Ability to communicate effectively in English (both written and oral). • Demonstrated experience and proficiency with MS Office word processing, spreadsheet, presentation, and database applications. Desired Characteristics 1. Minimum of 3 years experience medical device regulatory affairs. 2. Advanced degree in scientific, technology or legal disciplines 3. Regulatory Affairs Certification (RAPS) 4. Statistics education and or training 5. Ability to work independently in fast-paced environment with little supervision. 6. Ability to adapt to constant change and influence positive change effectively. 7. Team-oriented and responsive to customer needs. 8. Attention to Detail and Results-Oriented. 9. Ability to understand technical documentation and execute associated procedures About Us GE is the world's Digital Industrial Company, transforming industry with software-defined machines and solutions that are connected, responsive and predictive. Through our people, leadership development, services, technology and scale, GE delivers better outcomes for global customers by speaking the language of industry.

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医务经理 国药控股和记黄埔医药（上海）有限公司 重庆 5-8千/月 10-18

学历要求：大专|工作经验：2年|公司性质：合资|公司规模：150-500人

1. 负责重庆、贵州区域医院开发工作；2. 组织相关学术会议；3. 负责销售部门开发和维护消费者讲座讲课医生；4. 完成公司交待的其他工作。任职资格：1. 临床医疗、中医、护理类相关专业，大专及以上学历；2. 1年以上医药、医疗或母婴保健品类相关行业医务推广工作经验；3. 举止言谈得体，乐观、开朗，擅长与人沟通，具有敬业精神和开拓能力；4. 适应能力强，能承受一定的工作压力.

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无菌制剂操作员 阿斯利康药业（中国）有限公司 无锡-无锡新区 10-18

学历要求：大专|工作经验：1年|公司性质：外资（欧美）|公司规模：1000-5000人

工作职责：1. 生产活动- 遵守GMP, 按照SOP要求进行操作- 根据看板生产指令进行生产 - 及时完成BPR及使用日志，并汇报偏差 - 生产线清场 - 关注设备的运行状态，及时汇报异常状况 - 协助机修人员完成设备维修及维护保养 - 能够独立处理简单的设备故障、安装拆卸部件 2. 清洁活动 - 按照要求对物料及厂房进行清洁消毒 3. SHE - 承担个人安全职责，保护自己，并避免伤害他人和环境- 参加该岗位的必须的安全培训并配合应急预案的演练- 严格执行岗位安全操作规程- 及时汇报工作中的任何事故事件和危险源任职要求：1. 高中及以上学历2. GMP知识及无菌操作技能 3. 制药企业2年以上生产操作经验 4. 一定的英语读写 (学习) 能力 5. 基本的电脑操作技能6. 发现问题及解决故障的能力

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医药代表-呼吸/肝炎/中枢神经/血栓-辽宁大连 葛兰素史克（中国）投资有限公司 大连 6-8千/月 10-18

学历要求：大专|工作经验：1年|公司性质：外资（欧美）|公司规模：

1.在指定区域的目标医院中进行专业拜访和学术研讨活动，并达到公司要求。同当地医院的客户发展健康的工作关系并使其达到***化；2.主动参与专业技能及知识的学习，并达到公司要求，同时能有效地运用上述技能及知识于日常学术推广活动中；3.及时了解并收集客户疾病诊疗及品牌使用信息，按要求准时并如实地递交各种报表；4.积极参与公司的各种业务会议及团队建设，与团队共享专业推广经验、心得及市场信息，协助主管实现团队目标；5.通过积极参与SFA项目的实施，按要求及时准确录入相关信息（拜访、覆盖率、会议、客户拜访及医学信息提供的质量等），协助主管或经理确保系统的有效运作，并能够在数量及质量上得到检查及评估；6.协助主管/经理确保每个品牌的学术研讨活动与市场发展策略紧密相连；7.执行主管/经理制定的地区业务计划，制定并不断改进指定区域的业务计划；8.确保所有承担的活动完全符合公司的政策及质量标准，符合中华人民共和国的法律法规及其他相关的行为准则；9.完成上级要求的各项任务。任职要求：1、医学、药学或相关专业大专及以上学历，优秀应届生可考虑；2、良好的沟通与表达能力；3、有进取心，积极主动；4、有从事药品销售相关经验者优先。

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客户专员-肾科腹透产品（郑州） 百特（中国）投资有限公司 郑州 6-8千/月 10-18

学历要求：大专|工作经验：2年|公司性质：外资（欧美）|公司规模：500-1000人

关于百特百特提供多样化的核心肾脏和医院产品线，包括家庭治疗、急重症和中心透析治疗;无菌静脉解决方案;注入系统和设备;肠外营养;手术产品和麻醉学手术;自动化药房，软件和服务。百特在全球的足迹和对产品和服务的关键作用在扩大新兴和发达国家的医疗保健方面发挥了关键作用。百特全球员工基于公司丰富的医学突破的传统上正在促进下一代的员工创新医疗让病人得到照顾。你将会做的是很难列出你在百特要做的每件事因为每天都不同，但有些事很清楚是你要做的：负责肾科腹透产品在目标医院的开发，临床及病人的维护您是否具备在百特任职的资质?[任职资质] 临床医学，护理或相关专业本科学历；2-4年医药行业销售工作经验；有外企经验者优先；有临床医学或护理经验者优先；具有亲和力和较强的沟通能力； 诚实，工作踏实，责任心强；有很强的学习意愿和能力。为何选择百特？这是一项重要的事业 百特员工以拯救生命，延续生命为使命。我们充满激情，运用科技创新满足全球数以百万计人们的需求，他们依赖于百特医疗设备，技术和医疗必需品延续生命。我们致力于让越来越多的人接触到医疗保健，在重要的未知领域开拓创新，追求创新性的合作，以此来实现我们的使命以及对患者的承诺。立即申请职位，体验这一充满使命的职业！在百特每个员工享有均等的机会。员工不会因为种族，肤色，宗教，性别，性取向，国籍任何招聘决策，特有地位保护，残疾或其他受到法律保护的因素受到歧视。百特是一个机会均等的雇主，不会因为种族、肤色、宗教、性别、性取向、性别、国籍、受保护的退伍军人地位、残疾或任何其他受法律保护的情况影响招聘决定。

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