天津招聘

职位描述：
Job Purpose 岗位目的:
? Ownership of processes in the manufacturing and packaging facilities including process capability, process improvement initiative, process problems ownership and trouble-shooting.

Key Responsibilities主要岗位职责:
1. Prioritize work efforts to meet goals.
2. Maintain production document (Batch master record/SOP/Procedure/Form etc) related with routine production.
3. Enhance the Process understanding for the manufacturing and packaging processing which include process robustness study, initiate process improvement, and carry out trial and process validation.
4. Lead investigation and trouble shooting for issues, deviations/incident, customer complaint and failures, and evaluate the effectiveness of corrective actions to ensure no recurrence.
5. Draft, review and execute related validation documentation related to manufacturing and packaging process.
6. Provide support for the Annual Product Review and understand the process capability and implement improvement plan.
7. Provide routine support for the site in term of QMS implementation, and BOM, response to regulatory or customer request.
8. Establish, maintain and develop good relationships with other departments and make the communication smooth and effective.
9. Perform other jobs assigned by Process Section Manager.
10. 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.

Scope责任范围(Budget, Team Management 预算，团队管理)：
1. Accountable for maintain production document related with routine production.
2. Accountable for investigation and trouble shooting for issues, deviations and failures.
3. Accountable for process validation/evaluation protocol and report.


Impact & Risk 影响和风险: Directly contribute to routine production

Independence独立性(Decision Making 作决定)：

? Make the following decisions after the approval of line manager:
- Process improvement change
- Maintain document related with routine production

1. Bachelor or above education in engineering, science or pharmaceutical or related background.
2. At least 3 years experience in pharmaceutical manufacturing environment
3. Good process understanding knowledge and good analytical skills.
4. Good knowledge and understanding of GMP requirement
5. Knowledge and understanding of complex manufacturing and packaging processes
6. Standards of hygiene, quality, housekeeping required
7. Controlling of documentation.
8. Good communication and interpersonal skill, Good leadership
9. Good English level including oral communication, writing and listening
10. Good computer skills 举报 分享

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、***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***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。