Bioprocessing Specialist (DSP) in New Jersey

The role will involve performing downstream manufacturing to assure that the process is robust, scalable, and able to be performed in the manufacturing facility – as well as the accompanying documentation. The successful candidate will be familiar with cGMP regulations and technology transfer tasks and work out of the brand-new state-of-the-art facility in New Jersey, USA.

This position requires great attention to detail, ability to work in a team environment and a keen interest in optimisation of processes. Scientists will be responsible for adhering to all Quality Management System procedures, safety policies, and relevant parts of cGMP.

Responsibilities:

• Perform as a key member of the Downstream Manufacturing team, liaising with Process development and QA teams 
• Design and optimize downstream processing steps, including DNA purification techniques such chromatography, tangential flow filtration and formulation
• Wide...