Today Lonza is a global leader in life sciences. We are more than 15,000 employees in more than 100 locations around the world. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.

Lonza is establishing a strategic biomanufacturing base in China using GE Healthcare Solutions. With the new facility, Lonza is responding to growing demand for a high-quality CDMO in the Chinese market.

Key responsibilities:

• To perform hands-on laboratory work in the cell line and upstream process development team contributing to the development of processes suitable for technology transfer to the cGMP manufacturing teams. An understanding of cGMP manufacturing facility constraints and their impact on development activities will be developed.
• Contribute to process validation / characterisation activities by performing supporting laboratory scale studies, employing DoE methodologies.
• Interpret analytical data provided by the analytical team to define subsequent steps.
• Deliver high quality communication to ensure an outstanding customer experience (written reports, teleconferences, face-to-face meetings).
• Working as part of a site and global project team, co-ordinate multiple projects and ensure timely delivery of project workstages.
• Mammalian cell culture processes include: Cell Line Development (routine cell culture, FACS); Process Development (ambr15 miniturised bioreactors, 10L laboratory scale bioreactors); Process Characterisation (ambr250 miniturised bioreactors, 10L laboratory scale bioreactors).
• To work to the highest scientific standards under the direction of the Line Manager.
• To communicate project updates to internal and external customers.
• To contribute to the efficient running of the department including instigating and delivering operational efficiency projects.
• Contribute to departmental safety and training programmes as required.

Key requirements:

• PhD in a relevant Science field or Equivalent.
• Understanding of the theory and application of recombinant protein expression using mammalian cell culture systems.
• Understanding of cGMP regulations.
• Good problem solving, analytical and teamworking skills.
• Good communication skills (verbal and written).
• Accept weekend working on a rota based system, guarantee at least 3 working days every week

龙沙（中国）投资有限公司成立于2003年9月，是瑞士龙沙集团全资在广州设立的投资性公司。公司旨在于医药、化工及生命科学领域进行投资和再投资，同时提供以下服务：

-协助或代理龙沙所投资企业的货物及设备采购业务，并在国内外市场销售他们的产品；

-为龙沙所投资企业提供售后服务、技术支持及人力资源服务；

-为投资者提供咨询服务并为龙沙的关联公司提供市场信息、投资政策等咨询服务。