Medicine Fellow
苏州西艾信息咨询有限公司
- 公司规模:少于50人
- 公司性质:合资(非欧美)
- 公司行业:专业服务(咨询、人力资源、财会)
职位信息
- 发布日期:2013-10-15
- 工作地点:苏州
- 招聘人数:若干
- 工作经验:五年以上
- 学历要求:硕士
- 语言要求:英语精通
- 职位类别:医药技术研发管理人员
职位描述
Requirements:
? Advanced degree in a scientific or relevant discipline (Ph.D. or equivalent). And Minimum: MS or equivalent
? Good knowledge of English (oral and written). Desirable knowledge of site language.
? Successfully demonstrated several years (mini-mum of 3 years) of directly related experience as principal scientist or equivalent.
? Recognized expertise in a specific area.
? Proven track record in utilization of special tools/equipment, lab automation tools and spe-cialized facilities e.g., containment/sterile labs.
? Thorough knowledge of state-of-art instrumentation/equipment for broad field of applications.
? Thorough understanding of development processes in a specific function.
? Profound literature search skills.
? Ability to work in and/or lead interdisciplinary and/or cross-cultural teams.
? Proven leadership skills.
? Strong knowledge of relevant SOP, GLP, GMP and Novartis regulations and policies.
? Strong communication skills. Strong presentation skills and scientific/technical writing skills. Advanced coaching skills.
? May require up to 15% travel
Job Descriptions:
? Actively participate in teams, projects, networks and/or platforms. Fulfill all related tasks and responsibilities related to own discipline.
? Proactively communicate key issues and any other critical topics in a timely manner to the appropriate management level and/or to any other relevant project team member(s).
? Design, plan, perform and monitor all assigned activities.
? Ensure quality, quantity and timelines in all assigned projects, networks and/or platforms.
? Support and assign associates in specific projects and/or networks. Coach on target dates and priorities.
? Proactively participate in budget forecast, grant preparation and tracking of invoices. Ensure costs and cost awareness in all assigned projects and/or networks.
? Advise team members and work according to appropriate SOP's, GLP, GMP, OQM, HSE, ISEC and Novartis guidelines.
? Interpret results, evaluate data, draw relevant conclusions and write reports.
? Contribute to optimization of scientific/technical activities in assigned projects, network and/or platforms. Contribute to optimization of processes within the own area of responsibilities.
? Contribute to risk analyses and/or peer review and process challenge meetings.
? Generate and select most appropriate scientific documents to hand over to internal and/or external partners (TechOps, authorities, other companies) and proactively support generation of international registration documents. Interact with authorities where appropriate.
? Interact/collaborate with Research and/or other functions in Development to facilitate transfer of knowledge and deliveries of DS and/or DP.
? Actively support TRD as a technical expert on audits, inspections and/or Due diligence teams. Provide quality assessment of potential in-licensing products in a timely manner and support follow-up activities as appropriate.
? Proactively contribute to setting, updating and monitoring of team goals. Translate team goals into daily work.
? Support and facilitate the journey towards a multi-skilled, highly innovative and motivated workforce operating in a self-directed team set-up. Drive cultural evolution and change management. Support a culture of exceptional performance and continuous improvement, enabling innovative, competitive, compliant and consistent delivery on objectives of teams, projects, networks and/or platforms.
? Inspire/coach/lead team members: support objectives setting, performance evaluations, development planning discussions and ensure all related tasks (objectives entered, help to identify needs for training courses and development of new skills, etc.) are performed appropriately. Participate in recruiting process.
? Act as a role model in accordance with Novartis Values and Behaviors
? Identify and drive implementation of new scientific technologies and approaches.
? Provide efficient and robust processes for the manufacture and/or analysis of intermediates, drug substance and drug product as per own discipline.
? Report and present scientific/technical results internally and publish/present externally in scientific journals and conferences including patents.
? Ensure maintenance of infrastructure/equipment and required investments.
? Advanced degree in a scientific or relevant discipline (Ph.D. or equivalent). And Minimum: MS or equivalent
? Good knowledge of English (oral and written). Desirable knowledge of site language.
? Successfully demonstrated several years (mini-mum of 3 years) of directly related experience as principal scientist or equivalent.
? Recognized expertise in a specific area.
? Proven track record in utilization of special tools/equipment, lab automation tools and spe-cialized facilities e.g., containment/sterile labs.
? Thorough knowledge of state-of-art instrumentation/equipment for broad field of applications.
? Thorough understanding of development processes in a specific function.
? Profound literature search skills.
? Ability to work in and/or lead interdisciplinary and/or cross-cultural teams.
? Proven leadership skills.
? Strong knowledge of relevant SOP, GLP, GMP and Novartis regulations and policies.
? Strong communication skills. Strong presentation skills and scientific/technical writing skills. Advanced coaching skills.
? May require up to 15% travel
Job Descriptions:
? Actively participate in teams, projects, networks and/or platforms. Fulfill all related tasks and responsibilities related to own discipline.
? Proactively communicate key issues and any other critical topics in a timely manner to the appropriate management level and/or to any other relevant project team member(s).
? Design, plan, perform and monitor all assigned activities.
? Ensure quality, quantity and timelines in all assigned projects, networks and/or platforms.
? Support and assign associates in specific projects and/or networks. Coach on target dates and priorities.
? Proactively participate in budget forecast, grant preparation and tracking of invoices. Ensure costs and cost awareness in all assigned projects and/or networks.
? Advise team members and work according to appropriate SOP's, GLP, GMP, OQM, HSE, ISEC and Novartis guidelines.
? Interpret results, evaluate data, draw relevant conclusions and write reports.
? Contribute to optimization of scientific/technical activities in assigned projects, network and/or platforms. Contribute to optimization of processes within the own area of responsibilities.
? Contribute to risk analyses and/or peer review and process challenge meetings.
? Generate and select most appropriate scientific documents to hand over to internal and/or external partners (TechOps, authorities, other companies) and proactively support generation of international registration documents. Interact with authorities where appropriate.
? Interact/collaborate with Research and/or other functions in Development to facilitate transfer of knowledge and deliveries of DS and/or DP.
? Actively support TRD as a technical expert on audits, inspections and/or Due diligence teams. Provide quality assessment of potential in-licensing products in a timely manner and support follow-up activities as appropriate.
? Proactively contribute to setting, updating and monitoring of team goals. Translate team goals into daily work.
? Support and facilitate the journey towards a multi-skilled, highly innovative and motivated workforce operating in a self-directed team set-up. Drive cultural evolution and change management. Support a culture of exceptional performance and continuous improvement, enabling innovative, competitive, compliant and consistent delivery on objectives of teams, projects, networks and/or platforms.
? Inspire/coach/lead team members: support objectives setting, performance evaluations, development planning discussions and ensure all related tasks (objectives entered, help to identify needs for training courses and development of new skills, etc.) are performed appropriately. Participate in recruiting process.
? Act as a role model in accordance with Novartis Values and Behaviors
? Identify and drive implementation of new scientific technologies and approaches.
? Provide efficient and robust processes for the manufacture and/or analysis of intermediates, drug substance and drug product as per own discipline.
? Report and present scientific/technical results internally and publish/present externally in scientific journals and conferences including patents.
? Ensure maintenance of infrastructure/equipment and required investments.
公司介绍
当你十年寒窗苦读毕业,怎样接轨社会开启自己成功的职业生涯?当你认真工作,努力向上可曾想过应该再弥补些什么知识? 当你的同事获得提升而不是你的时候,你可知道自己哪里做的不到位?当你郁闷无比,又无法直抒胸臆时应该怎样主动解决当前状况?
人生的机遇充满了选择、惶惑与挑战, 什么才是最适合自己的路?-- 临渊羡鱼,不如退而结网
苏州西艾信息咨询有限公司,是一家从事职业规划,中高级猎头、背景调查、整体招聘解决方案以及企业管理咨询的专业机构,我们致力服务各类企业团队建设,并积极为个人提供职业发展规划建议以及能力提高的方式方向指导。客户与候选人的双赢是我们追求的永恒目标。我们服务过的行业包括快速消费品,化工,半导体,IT, 医药, 工业,装配生产以及研发领域。西艾咨询将坚持遵循高度的职业伦理,秉承“合作、高效、客观”的作风,为企业和职场人提供更为优质的服务。
西艾咨询的愿景:
成为口碑最好的职业规划平台
做优质企业与人才的最佳桥梁
西艾咨询的主要服务内容包括:
职业规划
中高级猎头服务
背景调查
整体招聘解决方案
性格与高考志愿选择服务
Email: hr@3L-consulting.cn
人生的机遇充满了选择、惶惑与挑战, 什么才是最适合自己的路?-- 临渊羡鱼,不如退而结网
苏州西艾信息咨询有限公司,是一家从事职业规划,中高级猎头、背景调查、整体招聘解决方案以及企业管理咨询的专业机构,我们致力服务各类企业团队建设,并积极为个人提供职业发展规划建议以及能力提高的方式方向指导。客户与候选人的双赢是我们追求的永恒目标。我们服务过的行业包括快速消费品,化工,半导体,IT, 医药, 工业,装配生产以及研发领域。西艾咨询将坚持遵循高度的职业伦理,秉承“合作、高效、客观”的作风,为企业和职场人提供更为优质的服务。
西艾咨询的愿景:
成为口碑最好的职业规划平台
做优质企业与人才的最佳桥梁
西艾咨询的主要服务内容包括:
职业规划
中高级猎头服务
背景调查
整体招聘解决方案
性格与高考志愿选择服务
Email: hr@3L-consulting.cn
联系方式
- Email:hr@3L-consulting.cnRequirements
- 公司地址:苏州工业园区东环路1500号现代创展大厦1109室
- 邮政编码:215021
- 联系人:西艾咨询
- 传真:(0512)62961203
- 电话:(0512)62720400