衡阳招聘

职位描述：
Job Purpose

Design, plan, perform, interpret scientific experiments to perform chemical and pharmaceutical profiling of NCEs resulting in robust analytical method development, solid form selection and formulation strategy development in collaboration within a multifunctional project team coordinated by a Project leader. Manage and contribute to maintenance of lab instruments/infrastructure.


Basic Major Activities

1. Meet quality, quantity and timelines in all assigned projects.
2. Design, plan and perform scientific experiments and plan, perform and contribute to project related scientific/technical activities under minimal guidance from more experienced team member (e.g., interpret and report results, generate and evaluate data, draw relevant conclusions, write reports).
3. Provide scientific and technical guidance. Coach team members as needed.
4. Provide efficient and robust processes for the solid form development, analysis and formulation development. Provide raw data documentation, evaluation and results interpretation. Propose and provide input for the design of next experiments.
5. Optimize existing methods (lab or plant) and develop more efficient ones.
6. Generate lab procedures, reports and/or instructions.
7. Actively transfer procedures/instructions to other functions, including troubleshooting, solid form optimisation, formulation scaleup etc.
8. Communicate and address problems, perform safety and literature searches under moderate guidance from more experienced team member.
9. Keep record of and manage chemicals, intermediates, excipients and solvents within own area of responsibility.
10. Collaborate with other team members to facilitate deliveries preclinical formulations.
11. Utilize special tools/equipments and/or specialized facilities e.g., containment facilities for potent compounds.
12. Generate scientific documents to hand over to internal and/or external partners (e.g., TechOps, authorities, external companies) and support generation of international registration documents under adequate guidance from more experienced team members.
13. Contribute to risk analyses and/or peer review and process challenge meetings.
14. Evaluate new lab equipment and prepare CAR and USR if applicable.
15. Report and present scientific/technical results internally and contribute to publications, presentations and patents.
16. Contribute to maintenance of infrastructure/equipment.
17. Actively contributes to team goals.






Key Performance Indicators


1. Adherence to costs, quality, quantity, and timelines for all assigned tasks.
2. Adherence to Novartis standards, in particular, quality, ethical, health, safety, and environment (HSE), and information security (ISEC) standards.
3. Feedback from other team members/leaders.
4. Refer to annual individual and team objective setting.
Measurable contributions to increasing efficiency and productivity in the work related to assigned projects.



Job Dimensions (Indicate key facts and figures)


Number of associates:
None
Financial responsibility:
(Budget, Cost, Sales, etc.)
None
Impact on the organization: Support own working unit by performing experiments/activities for on-time delivery of drug substance profiling, preclinical samples, procedures and processes.


Ideal Background

Education (minimum/desirable): Minimum: MS or equivalent degree in Pharmaceutical Analysis, Solid state chemistry or Pharmaceutics.

Desirable: PhD or equivalent.

Languages: Fluent in english and chinese (oral and written).
Experience/Professional requirement: 1. Minimum of 5 successful years of experience with MS degree or PhD from reputed university.
2. Awareness/proven experience for safe handling of chemicals, potentially dangerous materials and equipment.
3. Good scientific or technical knowledge in a specific area (e.g. Solid state, analytical, formulation).
4. Adequate knowledge in scientific/technical areas of collaboration.
5. Proficient with laboratory and/or technical tools.
6. Adequate knowledge of software and computer tools.
7. Basic presentation skills and scientific/technical writing skills.
8. Good Communication skills 举报 分享

北京诺华制药有限公司开发、生产和销售治疗多种疾病的创新处方药，涵盖的疾病领域包括：心血管、内分泌、肿瘤、抗感染、风湿疼痛及骨质疏松、移植免疫、中枢神经以及眼科。北京诺华制药曾获得“***雇主”和“最负社会责任的企业”等殊荣。

“诺华”中文取意“承诺中华”，即承诺通过不断创新的产品和服务致力于提高中国人民的健康水平和生活质量。北京诺华制药成立于1987年，总部设在北京，隶属于瑞士诺华公司。

诺华公司致力于为患者及社会提供创新医药保健解决方案，以满足其日益变化的健康需求。2011年，集团持续经营业务实现净销售586亿美元。集团研发投入约为96亿美元（去除减值及摊销后为92亿美元）。诺华集团总部位于瑞士巴塞尔，业务遍及全球140多个国家和地区，拥有124,000位全职员工。诺华集团立足在中国的长期发展，重要战略投资包括位于上海的综合性生物医学研发中心，以及位于北京昌平的制剂生产工厂和江苏常熟的原料药生产工厂。如需更多信息，敬请登录公司网站http://www.novartis.com和http://www.novartis.com.cn。