延吉招聘

Major Activities
1. Act as single point of contact and advisor for Guangdong Coastal Drug Institute, Guangzhou coastal drug institute and Zhuhai drug institute. Provide the test intelligence and knowledge of update Pharmacopoeia, registration standard etc
2. Set up quality control objective and system and ensure the sampling procedures, testing procedures and other quality management SOPs well followed in both labs and continuously improve the quality standard and test lead time
3. Lead quality control team in compliance with cGMP and ensure team capabilities by proper orientation training and continuous training according to the personnel needs and quality requirements
4. Establish the specifications and analytical method of the raw materials, excipients, packaging materials, bulk products, intermediate products and finished products, process water and environmental monitoring samples in compliance with Pharmacopoeia or registered dossier or internal UCB standard etc and ensure the methods validated
5. Manage the materials and products sampling, testing and completion of all required tests, ensure test records documented and reports reviewed and issued in time and accurate
6. Report the deviation or out of specification results to QA and ensure deviations and out of specification results properly investigated and corrective actions properly taken.
7. Maintain enough retained samples and ensure the execution of stability studies and provide stability study report
8. Follow the procedures to qualify, maintain, calibrate and retire the lab instruments, make sure the instrument qualified and calibrated.
9. Manage the reagents, reference standards, testing solutions, strains and culture media and make sure compliance with standards and shelf life.
10. Participate the annual product quality review and periodic assessment of procedure and activities
11. Participate the complaint investigation and customer audit
12. Participate and support the process validation, cleaning validation and environmental monitoring activities

Personal requirement:

1 Good Knowledge in theory and practice, licensed pharmacist
2 Above Bachelor degree, major in pharmacy or chemistry or biologic
3 More than 10 years pharmaceutical experiences, at least 5 years experiences in quality control chemical lab, multinational pharmaceutical experience preferred
4 Good interpersonal and communication skills
5 Good leadership and management skills
6 Fluent English
7 Familiar with cGMP, ICH and Chinese Pharmacopoeia etc

比利时优时比制药公司（UCB）始建于1928年，总部设在比利时布鲁塞尔，在英国伦敦Slough和剑桥等地拥有2个研发中心。在八十年的发展中，优时比制药公司致力于为重症患者提供更多的创新治疗方法，造福人类。 优时比制药在全球业务遍布40多个国家，拥有近一万名员工。2010年全球销售收入32亿欧元。全球百强医药行业排名第33位。随着业务的不断拓展，2004年5月，优时比制药完成了对英国生物制药企业--细胞技术公司的收购。2007年9月1日，又完成了对德国许瓦兹制药集团的全球并购。至此，优时比制药公司成功地实现了全球领先的生物制药公司的战略定位。
优时比制药在华机构包括优时比贸易（上海）有限公司和珠海许瓦兹制药有限公司，业务遍及全国，产品涉及中枢神经系统疾病、变应性疾病、心血管疾病、贫血和疼痛治疗等领域。
创新、开拓、诚信、尽责、关爱、包容与业绩是优时比制药公司始终遵循的价值观。
面向未来，比利时优时比制药公司一如既往地秉承特有的业绩、尽责、诚信、包容、关爱、开拓和创新的价值观和企业文化，将建设一个全球生物医药的领先者，首要任务是带来专家和新药，治疗各种严重疾病的患者。
    
公司网站：******************
中文网站：************************

为什么选择我们？

卓越完善的人才发展战略
优时比业务的多样性和国际化为其员工提供了广阔的个人发展平台。员工一旦加入我们，就会得到公司在培训、业绩表现和个人潜力挖掘等方面提供的帮助。无论您的专业和职务是什么，您都将对自己的发展前景了然于胸。我们不仅提供正规的培训，而且还通过精良的个人发展计划和在职培训等途径为您的前途指路。

有竞争力的薪酬体系
从长远来看，为了吸引人才，保留人才，并激励人才，我们确保所提供的薪资福利具有市场竞争力。我们期待着员工能有优秀的表现并得到优厚的回报，因而把薪资和员工对公司的贡献直接联系起来。
上海总公司地址：上海市西藏中路268号来福士广场办公楼2802室

欢迎有意向的候选人可将简历投递至邮箱：chinacampus@ucb.com。应聘简历请在主题中注明申请职位名称。