Seeking experienced Process Engineer with specific experience in preformulation testing, formulation development, and manufacturing process development for small molecule drugs in tablet, capsule, or similar dosage forms (to include granules, powders, sachets, chewables, etc.).
The position requires high energy and a willingness to make process improvements based on data and investigation. The individual will conduct methodical reviews of existing processes in order to improve quality, consistency of the build processes, throughput, and lead times.
In this role, you will be providing technical input in the selection, specification, test, screening, qualification, application, and root cause failure analysis of electronic parts, materials, and processes (PM&P).
Evaluate process parameters such as: Drying time and temperature; Heating and cooling rates; Component mixing order, speed, and time; Addition rate for solvents, excipients, granulating agents, API, etc.; Filter size (liquids) and screen size (solids).
This position will provide technical support to the Engineering Department for the Riverside facility and global suppliers for the purpose of development of processes, and/or material data base qualifications.
This role will include technology and device development at a foundry, TCAD simulations, RF and DC device characterization, and layout optimization using innovative device concepts to deliver next generation performance.
In this role, you will interacts with site and corporate functions to assess the scientific, regulatory, and business impact of process improvement initiatives. Assists in the management and implementation of approved process improvement projects at the IMF.
Review injection molding design of experiments, viscosity study, gate freeze study, CPK, and inspection data, discuss out of spec dimensions with the engineers and tool makers, so that corrective action can be implemented.