USP Bioprocessing Specialist III

The role will involve performing upstream manufacturing to ensure that the process is robust, scalable, and successfully executed 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, the ability to work in a team environment, and a keen interest in the optimization of processes. Scientists will be responsible for adhering to all Quality Management System procedures, safety policies, and relevant parts of cGMP.

Location: On-site, USA - New Jersey

Type: Full-time

Responsibilities:

• Optimize bioreactor performance and scale-up procedures to meet production goals and maintain product quality.
• Develop and refine operating equipment specifications and...