湛江招聘

Job Purpose:

Perform Quality Audits of suppliers of pharmaceutical starting materials and packaging materials located in China and border countries, on behalf of quality department of Sanofi Industrial Affairs sites using these materials and located outside of the country.
Provide an independent quality assessment of the audited suppliers

Responsibilities:
- Organize, Plan and Perform Quality Audits of suppliers, upon request from Industrial Quality & Compliance. Provide an assessment of quality in place with regards to material compliance, as well as regulatory and quality requirements. Identify gaps and area of improvement. Ensure the establishment of acceptable action plan (CAPA) to remediate identified deficiencies
- Being a local quality contact between the Suppliers, IQC-Suppliers and IA sites to facilitate follow up of improvements and exchange of quality information
- Participate to qualification of new auditors in the country, by performing audits with them and providing expertize regarding quality assessment of suppliers
- Support audits leaded by other auditors when specific expertize is needed (e.g.: for cause audit with user site representative, highly sophisticated topics)

Qualifications:
Scientific experience in Pharmaceutical and Chemical industry
Good operational knowledge of Quality regulations in a pharmaceutical environment: GMP, GTDP, ISO..
Operational Experience in at least one technical field: production or quality in pharmaceuticals, steriles, chemistry, biotechnologies, analytical, information systems, supply chain
Prior experience in the pharma regulated environment: manufacturing and testing, quality,
Fluent in English oral and written
Excellent ability to make a realistic diagnosis, question the evidence, challenge datas from different sources
Excellent ability to adapt quickly to unexpected situations, to reorganize priorities on the spot and adapt the audit conduct according to findings
Excellent listening skills, interpersonal skills, ability to manage conflict and step back
Ready to travel 50% of time

集团概况
赛诺菲集团是名列全球第三，欧洲第一的制药公司。集团拥有世界级的研发机构，约有11000名科学家在研究和开发着创新的治疗方案，其主要研究领域涉及心血管、血栓、肿瘤、中枢神经系统、糖尿病、内科和疫苗。

赛诺菲集团分别在法国巴黎和美国纽约上市。

赛诺菲集团的宗旨是:健康

集团的价值观
创新    鼓励前瞻思维    我们燃点创意
信心    卓然不群     我们胆识过人
尊重    求同存异     我们彼此尊重
齐心    恪守社会责任    我们勇于担当
正直    克己慎行     我们坚守承诺

赛诺菲杭州工厂前身杭州赛诺菲民生制药有限公司（中外合资企业）于1995年11月30日在杭州注册成立。

赛诺菲杭州工厂是赛诺菲中国六大生产基地之一，工厂员工160余人，公司生产和包装固体和口服制剂、包装针剂以，产品涵盖内科用药、中枢神经系统、高血压、心血管、血栓、肿瘤领域21种处方药以及4种OTC药物。

2009年4月，赛诺菲集团宣布投资4.29亿人民币，在杭州滨江高新技术产业开发区打造新的生产基地，并通过升级和技改现有设备，发展成为亚洲的出口加工基地。

杭州工厂目前在滨江新厂区办公。