Sr.scientist
CNIBR-诺华（中国）生物医学研究有限公司
- 公司性质：外资(非欧美)
- 公司行业：制药/生物工程
职位信息
- 发布日期：2013-07-26
- 工作地点：常熟
- 招聘人数：1
- 学历要求：博士
- 职位类别：医药技术研发人员
职位描述
Job Description:
? Apply modern analytical technologies (e.g. HPLC, GC, auto-titration and NMR, IR, UV) to develop fast and robust analytical methods for monitoring of synthesis reactions, identification and structural elucidation of impurities and, and purity analysis.
? Follow defined quality standards (technical to GLP/GMP) to perform method validation, sample testing, release and in-process control for manufacture of intermediates and active pharmaceutical ingredients (APIs) with high quality documentation delivered in a timely manner.
? As a team member, join project team meetings and discussions and provide valuable inputs for establishment of project strategy and development plan and technical problem solving. Estabish sophisticated analytical R&D development plan and provide efficient analytical R&D support to ensure successful delivery of all assigned projects on time.
? Perform maintenance, calibration and troubleshooting of analytical instruments and equipment and keep daily operations in good HSE and quality compliance by following internal guidelines and procedures.
? Proactively contribute to the organizing and management of analytical labs to maintain efficient and smooth operations of analytical labs.
? Be a proactive contributor to continuous improvement of internal processes and technical excellence.
Requirements:
? Ph.D. or M.S. in analytical chemistry, or organic chemistry or other closely-related education background with sound analytical chemistry knowledge, five or more years of experience in pharmaceutical industry or equivalence is preferable.
? Results driven, highly committed and accountable with excellent organizing and planning skills.
? Very good teamworking skills with good leadership.
? Proficient in MS Windows and MS Office & chemistry applications software.
? Proactive and self-motivated team player with good interpersonal communication.
? Fluent English reading and writing is a must and fluent oral English preferred
? Apply modern analytical technologies (e.g. HPLC, GC, auto-titration and NMR, IR, UV) to develop fast and robust analytical methods for monitoring of synthesis reactions, identification and structural elucidation of impurities and, and purity analysis.
? Follow defined quality standards (technical to GLP/GMP) to perform method validation, sample testing, release and in-process control for manufacture of intermediates and active pharmaceutical ingredients (APIs) with high quality documentation delivered in a timely manner.
? As a team member, join project team meetings and discussions and provide valuable inputs for establishment of project strategy and development plan and technical problem solving. Estabish sophisticated analytical R&D development plan and provide efficient analytical R&D support to ensure successful delivery of all assigned projects on time.
? Perform maintenance, calibration and troubleshooting of analytical instruments and equipment and keep daily operations in good HSE and quality compliance by following internal guidelines and procedures.
? Proactively contribute to the organizing and management of analytical labs to maintain efficient and smooth operations of analytical labs.
? Be a proactive contributor to continuous improvement of internal processes and technical excellence.
Requirements:
? Ph.D. or M.S. in analytical chemistry, or organic chemistry or other closely-related education background with sound analytical chemistry knowledge, five or more years of experience in pharmaceutical industry or equivalence is preferable.
? Results driven, highly committed and accountable with excellent organizing and planning skills.
? Very good teamworking skills with good leadership.
? Proficient in MS Windows and MS Office & chemistry applications software.
? Proactive and self-motivated team player with good interpersonal communication.
? Fluent English reading and writing is a must and fluent oral English preferred
公司介绍
诺华（Novartis AG）是全球医药保健行业的领导者。其核心业务涉及专利药，非专利药，眼睛护理，消费者保健和动物保健等领域。诺华公司总部设在瑞士巴塞尔，业务遍及全球140多个国家和地区。
诺华（中国）生物医学研究有限公司是诺华全球研发组织――诺华生物医学研究所（NIBR）的第八个研究基地。我们位于中国上海市张江高科技园区，将成为诺华在亚洲的主要研究中心，以及除在欧美的研究中心外的最主要的研究中心。我们的研究和探索开发活动的重点是发现并开发创新疗法，用于治疗在亚洲远未达到医药需求的疾病。我们与从不同之处在于将专注现代药物的发现和开发方法的研究。最初阶段，研发工作将专注在引起中国地方性癌症的感染原因。我们还将开展临床试验，进行安全性研究，生物标志物和检测分析，表达谱、生物分析以及转化医学的研究。
随着公司业务的迅速扩展，我们热忱欢迎您的加入。同时我们将提供具有竞争力的薪酬福利待遇以及良好的培训发展机会。
诺华（中国）生物医学研究有限公司是诺华全球研发组织――诺华生物医学研究所（NIBR）的第八个研究基地。我们位于中国上海市张江高科技园区，将成为诺华在亚洲的主要研究中心，以及除在欧美的研究中心外的最主要的研究中心。我们的研究和探索开发活动的重点是发现并开发创新疗法，用于治疗在亚洲远未达到医药需求的疾病。我们与从不同之处在于将专注现代药物的发现和开发方法的研究。最初阶段，研发工作将专注在引起中国地方性癌症的感染原因。我们还将开展临床试验，进行安全性研究，生物标志物和检测分析，表达谱、生物分析以及转化医学的研究。
随着公司业务的迅速扩展，我们热忱欢迎您的加入。同时我们将提供具有竞争力的薪酬福利待遇以及良好的培训发展机会。