QC Technical Supporting Lead实验室技术支持
职位描述
Key Responsibilities主要岗位职责:
? Project
1. Qualification of Test method and equipment used in QC lab qualification to ensure they are validated and compliance with regulatory requirements. Prepare analytical method validation protocol, implement the validation plan and write summary report
2. All CAPEX could be well control and tracked to assure the equipment capability is suitable for working load and they are available on schedule.
3. Product project: to ensure all the actions relative to product project (Technical) are well planed and completed on schedule;
4. Communicate with other sites, i.e. Aranda, Jurong, Bad Oldesloe, Poznan and Boronia
5. Maintenance the API 100 information relative to QC.
6. Improve the knowledge of CDS system of QC staff
? Daily responsibility
7. Obey vocational moral and GMP/GLP disciplines strictly, ensure the test results are accurate and reliable
8. Report any atypical or out of specification test result, investigate and find out root cause
9. Prepare new product registration relevant document and draft specification and test method
10. Implement or support the validation, calibration and maintenance of equipment in QC lab
11. Train new analysts
12. Support internal audits, GQA audits and regulatory inspection
13. When section manager is out of office, acts as deputy
14. Perform other jobs assigned by QC section manager
15. Understand and comply with the applicable local regulations of Quality, EHS and others, GSK standards for QMS, EHSS etc. and company policy. Adherence to standard operating procedures
16. Stability trending module SME
? EHS
17. Follow GSKT EHS policy and ensure safety and health during the work.
18. Responsible for reduction of lab waste and EHS risk, avoiding working injury.
19. Responsible for proper usage and effective management of virulent substances.
Qualifications:
? University graduate or higher in Pharmaceutical or related area.
? Minimum 3 years experience in Pharmaceutical or biological company.
? Knowledge of GMP, GLP and pharmacopoeia e.g. USP, EP. CP.
? Master chemical professional skill.
? Master analytical equipment operational and general maintenance skill.
? Good English listening, reading and writing skills.
? Proven good computer skills.
? Good interpersonal co-operator and communication skills.
? Preferable understanding of organization structure, business operation and company culture of GSK.
? Good initiative
? Leadership potential
Besides the above technical knowledge of laboratory analysis and operations, this position also requires the individual to have a good command of GPS principles and knowledge. This role requires strong leadership capabilities to interact with GPS experts in the GMS network, section supervisors and lab analysts.
企业简介
葛兰素史克公司在中国的历史最早可追溯至20世纪初叶。自20世纪80年代以来,在中国政府改革开放政策的感召下,公司在中国积极投资,将最先进的制药技术、最优质的产品、最新型的商业模式、最现代化的管理理念和市场营销技巧引入了中国。
葛兰素威康和史克必成公司于2000年12月完成全球性合并,2002年,葛兰素史克(中国)投资有限公司全面完成业务整合并正式宣布成立,成为中国目前规模最大的跨国制药企业之一。公司业务由处方药、非处方药、疫苗和消费保健品4大部分组成,投资公司和地区总部位于北京,主要业务中心分设在上海、天津和香港。
葛兰素史克是最早在中国成功兴建合资企业的外国制药公司之一。在进入中国的20多年间,葛兰素史克先后成立了5家公司,目前2家为合资企业,总注册资本超过2.3亿美元。目前公司在全国28个主要城市(包括香港)设立了办事机构,在全国拥有近3000名员工,为中国的医药行业培养了一大批高素质的商业管理人员和技术骨干。
天津相关职位: 医药信息沟通经理
热门区域招聘: 重庆 北京 上海 浙江 江苏 广东 山东 湖南 安徽 河北
天津招聘企业: 英集(天津)文化科技有限公司 青松医药集团股份有限公司 天津红日药业股份有限公司 天士力医药集团股份有限公司 天津华裕生物科技有限公司 天津畅润华生物科技有限公司 天津海金正略科技发展有限公司 天津红日康仁堂药品销售有限公司 天津远泰医药贸易有限公司 天士力医药商业有限公司
职位发布日期: 2017-12-04