Downstream GMP Manufacturing Associate

The Downstream GMP Manufacturing Associate will work as part of a team and work directly in activities associated with purification that applies a broad knowledge of biological, bioprocess, and mechanical principles to execute complex operations that result in clinical and commercial stage medicines to dramatically improve the human condition through gene therapy. The activities will take place in a cleanroom following aseptic techniques and procedures in a cGMP environment. Duties and Responsibilities Train on and perform Downstream purification activities such as Chromatography, Tangential flow filtration (TFF), Ultracentrifugation, and Final Formulation steps Work in cleanroom environment while adhering to Standard Operating Procedures (SOPs) and Batch production Records (BPRs) Prepare,