Sr. Manager, Process Development
苏州百特医疗用品有限公司
- 公司规模:500-1000人
- 公司性质:外资(欧美)
- 公司行业:制药/生物工程
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:本科
- 语言要求:英语熟练
- 职位类别:医药技术研发人员
职位描述
Job Descriptions:
1. Select, develop and retain team. Define and communicate criteria by which team and individual success will be measured. Provide constructive feedback and recognition. Successfully coach and motivate others for outstanding performance.
2. Manage team members to effectively develop manufacturing processes for pharmaceutical parenteral products and carry out technology transfer by using QbD principles.
3. Operate and maintain pilot lab facilities in Suzhou.
4. Solve problems expeditiously through the use of multiple disciplines and technical principles. Create innovative manufacturing processes by leveraging expertise within the organization.
5. Provide leadership to team members in terms of prioritization, problem resolution, referrals to appropriate experts, etc.
6. Understand strategic imperatives to project success (e.g. timing of market entry, innovative technology and costs). Develop strategic plans that incorporate regional and global business practices and customer needs.
7. Develop effective project milestones, schedules and manage budgets, including capital. Identify and resolve issues that may jeopardize project schedules or improve project time.
8. Seek regular input and feedback from customers and take appropriate action.
9. Proactively prioritize and balance utilization of resources allocated to project; identify opportunities to cross-train, back-fill. Develop recommendations for outside resources as required for the team/project; present internal vs. external analysis.
10. Ensure alignment of team objectives with business strategies. Deliver on commitment to project teams and manage budgets.
11. Build a professional network both internally within the business unit, across units and outside of Baxter.
12. Manage team members to effectively transfer technology from design development to implementation.
13. Maintain current knowledge of relevant Quality System Regulations and other regulatory requirements related to research and development (product development, design and safety) to ensure compliance in all research, data collection and reporting activities.
14. Must be able to travel for assignments.
Qualifications:
1. Must be well versed in scientific disciplines relevant to pharmaceutical parenteral products.
2. Must have working knowledge of GMPs, QbD and ICH and be familiar with expectations and practices of various regulatory agencies.
3. Must demonstrate strategic leadership and proficient supervisory skills.
4. Capable of analyzing and solving complex problems.
5. Must able to effectively manage team in a cross-functional matrix environment.
6. Display ability to communicate effectively with global teams, using a wide variety of skills and vehicles and to various audiences including senior management. Proficiency in Chinese and English is required. Ability to speak French is a plus.
7. Understanding of financial tools and ability to set budgets appropriately
8. Bachelors with at least 10 years experience, Masters with at least 8 years of experience, or Ph.D. with at least 5 years experience. The degree should be in Chemistry, Chemical Engineering, or Pharmaceutics/Pharmaceutical Engineering is required.
1. Select, develop and retain team. Define and communicate criteria by which team and individual success will be measured. Provide constructive feedback and recognition. Successfully coach and motivate others for outstanding performance.
2. Manage team members to effectively develop manufacturing processes for pharmaceutical parenteral products and carry out technology transfer by using QbD principles.
3. Operate and maintain pilot lab facilities in Suzhou.
4. Solve problems expeditiously through the use of multiple disciplines and technical principles. Create innovative manufacturing processes by leveraging expertise within the organization.
5. Provide leadership to team members in terms of prioritization, problem resolution, referrals to appropriate experts, etc.
6. Understand strategic imperatives to project success (e.g. timing of market entry, innovative technology and costs). Develop strategic plans that incorporate regional and global business practices and customer needs.
7. Develop effective project milestones, schedules and manage budgets, including capital. Identify and resolve issues that may jeopardize project schedules or improve project time.
8. Seek regular input and feedback from customers and take appropriate action.
9. Proactively prioritize and balance utilization of resources allocated to project; identify opportunities to cross-train, back-fill. Develop recommendations for outside resources as required for the team/project; present internal vs. external analysis.
10. Ensure alignment of team objectives with business strategies. Deliver on commitment to project teams and manage budgets.
11. Build a professional network both internally within the business unit, across units and outside of Baxter.
12. Manage team members to effectively transfer technology from design development to implementation.
13. Maintain current knowledge of relevant Quality System Regulations and other regulatory requirements related to research and development (product development, design and safety) to ensure compliance in all research, data collection and reporting activities.
14. Must be able to travel for assignments.
Qualifications:
1. Must be well versed in scientific disciplines relevant to pharmaceutical parenteral products.
2. Must have working knowledge of GMPs, QbD and ICH and be familiar with expectations and practices of various regulatory agencies.
3. Must demonstrate strategic leadership and proficient supervisory skills.
4. Capable of analyzing and solving complex problems.
5. Must able to effectively manage team in a cross-functional matrix environment.
6. Display ability to communicate effectively with global teams, using a wide variety of skills and vehicles and to various audiences including senior management. Proficiency in Chinese and English is required. Ability to speak French is a plus.
7. Understanding of financial tools and ability to set budgets appropriately
8. Bachelors with at least 10 years experience, Masters with at least 8 years of experience, or Ph.D. with at least 5 years experience. The degree should be in Chemistry, Chemical Engineering, or Pharmaceutics/Pharmaceutical Engineering is required.
公司介绍
特别注明:苏州百特的所有招聘岗位仅通过圆才网和前程无忧网进行发布和收集简历!苏州百特的联系地址只有一个,白榆路27号。
每一天,百特影响着数以百万计的生命,我们凭借必要的医院和肾科产品与服务应对重大健康需求。在全球,几乎每个医院的每个科室,乃至每一楼层,都能发现百特产品与疗法的身影。同时,百特也出现在诊所和患者家中。
Every day, Millions of lives relay on Baxter, Our products and service are essential building blocks of healthcare. Baxter products and treatment are found almost in everyplace, in every hospital at every Department even on every floor. Meanwhile, Baxter is there, not only the clinic but also our patient home.
百特于上世纪80年代来到中国,是***进入中国医疗市场的大型跨国医疗企业之一。秉承“拯救并延续生命”的企业使命,百特专注于协助提升医疗标准、扩大医疗可及性和回馈社会等关键性工作,为中国患者的生命和生活质量做出有意义的贡献,助力中国医疗事业的可持续发展。
In the 80s Baxter has come to China which is one of the earliest multinational medical enterprise, Our mission to save and sustain lives inspires our work and our commitment to expanding access to care, providing cost-effective healthcare solutions, delivering quality products and advancing innovations, also delivering contribution to our patient and their Quality lives meanwhile it will be supportive of sustainable development for Chinese medical treatment cause
苏州百特医疗用品有限公司成立于1995年, 是百特在中国建立的***家独资工厂,主要生产静脉输液袋、腹膜透析袋及相关组件,以用于静脉输注及腹膜透析治疗。我们始终严格执行中国质量管理体系,确保我们的产品以***质量和安全标准为患者及医护人员服务。目前, 560多名员工正运用最创新和先进的制造技术,为中国大陆、中国台湾、新加坡、澳大利亚、菲律宾及泰国等国家和地区的客户提供优质高效的医疗产品,为依赖于百特产品的患者带去有意义的改变。
Suzhou Baxter healthcare co., LTD is founded in 1995, This is the first sole plant in China. Baxter Suzhou produced venous transfusion container, PD bag and other related components which used in PD and venoclysis treatment, In order to provide the high-quality product, and let our customers using safety. Baxter Suzhou not only follow up the quality policy of Baxter headquarters, but also carry out the quality management system of China strictly as well ,At present, more than 560 employees are using the latest manufacturing technology to provide high quality medical products for customers comes from China Taiwan, India, Australia and the Philippines.
我们的理念是注重结果、客户导向;我们的价值观是正直诚实、坦诚沟通、承责力行;我们的激励方式是鼓励创新、奖励优秀。百特致力于成为危重治疗领域的领先企业,期盼更多优秀人才的加入,我们承诺为您提供充满活力的工作和成长环境,与百特共筑未来!
每一天,百特影响着数以百万计的生命,我们凭借必要的医院和肾科产品与服务应对重大健康需求。在全球,几乎每个医院的每个科室,乃至每一楼层,都能发现百特产品与疗法的身影。同时,百特也出现在诊所和患者家中。
Every day, Millions of lives relay on Baxter, Our products and service are essential building blocks of healthcare. Baxter products and treatment are found almost in everyplace, in every hospital at every Department even on every floor. Meanwhile, Baxter is there, not only the clinic but also our patient home.
百特于上世纪80年代来到中国,是***进入中国医疗市场的大型跨国医疗企业之一。秉承“拯救并延续生命”的企业使命,百特专注于协助提升医疗标准、扩大医疗可及性和回馈社会等关键性工作,为中国患者的生命和生活质量做出有意义的贡献,助力中国医疗事业的可持续发展。
In the 80s Baxter has come to China which is one of the earliest multinational medical enterprise, Our mission to save and sustain lives inspires our work and our commitment to expanding access to care, providing cost-effective healthcare solutions, delivering quality products and advancing innovations, also delivering contribution to our patient and their Quality lives meanwhile it will be supportive of sustainable development for Chinese medical treatment cause
苏州百特医疗用品有限公司成立于1995年, 是百特在中国建立的***家独资工厂,主要生产静脉输液袋、腹膜透析袋及相关组件,以用于静脉输注及腹膜透析治疗。我们始终严格执行中国质量管理体系,确保我们的产品以***质量和安全标准为患者及医护人员服务。目前, 560多名员工正运用最创新和先进的制造技术,为中国大陆、中国台湾、新加坡、澳大利亚、菲律宾及泰国等国家和地区的客户提供优质高效的医疗产品,为依赖于百特产品的患者带去有意义的改变。
Suzhou Baxter healthcare co., LTD is founded in 1995, This is the first sole plant in China. Baxter Suzhou produced venous transfusion container, PD bag and other related components which used in PD and venoclysis treatment, In order to provide the high-quality product, and let our customers using safety. Baxter Suzhou not only follow up the quality policy of Baxter headquarters, but also carry out the quality management system of China strictly as well ,At present, more than 560 employees are using the latest manufacturing technology to provide high quality medical products for customers comes from China Taiwan, India, Australia and the Philippines.
我们的理念是注重结果、客户导向;我们的价值观是正直诚实、坦诚沟通、承责力行;我们的激励方式是鼓励创新、奖励优秀。百特致力于成为危重治疗领域的领先企业,期盼更多优秀人才的加入,我们承诺为您提供充满活力的工作和成长环境,与百特共筑未来!
联系方式
- 公司地址:百特天津工厂