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

龍沙（中國）投資有限公司成立于2003年9月，是瑞士龍沙集團全資在廣州設(shè)立的投資性公司。公司旨在于醫(yī)藥、化工及生命科學(xué)領(lǐng)域進行投資和再投資，同時提供以下服務(wù)：

-協(xié)助或代理龍沙所投資企業(yè)的貨物及設(shè)備采購業(yè)務(wù)，并在國內(nèi)外市場銷售他們的產(chǎn)品；

-為龍沙所投資企業(yè)提供售后服務(wù)、技術(shù)支持及人力資源服務(wù)；

-為投資者提供咨詢服務(wù)并為龍沙的關(guān)聯(lián)公司提供市場信息、投資政策等咨詢服務(wù)。