Sr. Research Scientist (Particle)
科锐国际人力资源(北京)有限公司
- 公司规模:1000-5000人
- 公司行业:专业服务(咨询、人力资源、财会)
职位信息
- 发布日期:2013-12-17
- 工作地点:苏州
- 招聘人数:若干
- 学历要求:其他
- 职位类别:医药技术研发人员
职位描述
职责描述:
Summary: | Global technical leader in particle science and resource manager to oversee the prioritization and timely completion of particle identification and compendial particle analytical requests. This role requires documented contributions to technical interpretation of analytical data and root cause investigations that impact quality decisions related to product complaints, release of manufactured products, and enabling new product development. This role facilitates and integrates additional analytical tools/resources as needed and demonstrates strong communication skills during customer engagements. In addition to having an in-depth knowledge and understanding of GxP and regulatory requirements, this role helps develop the personnel, capabilities, and maintain state-of-the-art facilities. |
Essential Duties and Responsibilities: | · Contribute to strategic initiatives that drive value across division and businesses; participate on global task forces and committees; initiate exchange of technical information with other research groups inside and external to Baxter. · Act as technical expert in technical feasibility analysis where new and unproven methods and technologies are required. · Analyze technical and theoretical concepts and modify them to increase product/process acceptance, quality and reliability. · Develop state-of-the-art processes (design, quality improvements research techniques, etc.) that span multiple disciplines. · In addition to having an in-depth knowledge and understanding of GxP and related regulations and guidance, is able to provide expert insights into such regulations so as to facilitate efficient product registration and/or is an active participant in the generation, review, adoption and interpretation of such regulations. · Further recognition can be evidenced by presentations at external conferences, published articles in peer review journals and/or holding of multiple patents. |
要求:
Qualifications: | · Strong working knowledge around current and emerging global regulatory requirements for visual inspection, sub-visible particle characterization, and interfacing with regulatory bodies around particulate matter issues. · Experience with FTIR Microscopy, SEM and EDX analyses, light microscopy (including PLM), and light obscuration techniques for solution particle counting. · Skills in resource and project management, leading root cause investigations, and technical writing are required. |
Education and/or Experience: | · Bachelor's degree in a scientific discipline with at least 20 years, MS with at least 15 years or PhD with 8 years of relevant work experience. Research experience in GMP/QSR environment is essential. · Lab experience includes research the GMP/QSR environment, leadership of technical teams, and project management experience is desirable. |
公司简介:
于1931年在美国成立,是世界上知名的生产多种医疗器械及用品的跨国公司之一,总部设在美国芝加哥,在全球110多个国家设立了超过250家公司和分支机构,全球雇员总数约50,000人。生产、销售10万余种医疗产品,百特的宗旨是向最威胁人类生命的疾病提供至关重要的疗法,成为全球领先者。 在中国拥有多家独资及合资企业,成立了投资公司,并在北京、上海、广州、成都、香港等城市设立了办事机构,主要生产肾科、静脉输注和血液治疗制品。? 1995年,中国建立的第一家独资工厂。 苏州工厂座落于中国-新加坡苏州工业园区,距国际性大都市--上海仅86公里。公司主体建筑于1998年竣工,占地面积共22750平方米。目前,500多名员工正运用最新的制造技术为中国以及印度、澳大利亚和菲律宾等的客户提供高质量的医疗产品。主要生产静脉输液袋及腹膜透析袋及相关组件等用于静脉输注及腹膜透析。
正在苏州工业园建立其研发中心以支持全球业务的快速增长!* 研发是公司发展必不可少的内容之一。公司的各种技术专长是其最大的优势之一。公司独具匠心地综合利用本身在医疗器械、制药和生物技术方面的能力,使其在医疗保健行业公司中脱颖而出。公司的研发人员高度重视科技创新,他们与业务部门密切合作,开发出独特的新产品并改良现有产品,从而满足全球范围的关键医疗保健需求。