Perform chemical engineering related projects for the improvement of company’s medical device manufacturing process and quality control. Plan and implement laboratory test, pilot and plant investigations, and subsequent process control and quality control. Establish long-term optimum process control parameters for compounding, solution filling process and polypropylene extrusion process by applying mass transfer, heat transfer and chemical engineering techniques. Contribute to solving of complex problems related to process, mechanical, quality, equipment integrity and other disciplines. Participate in incident investigations and cause analysis for Quality, Reliability, Production, Safety and Environmental. Implement corrective and preventive action (CAPA) and ensures that the CAPA is documented and executed. Establish Standard Operating Procedures in compliance with ISO and cGMP regulations and participate in FDA, ISO and client’s on-site quality audits.
Master’s Degree in Chemical Engineering required.
At least 1 year experience in industry or academic in analytical chemistry testing and microbiology laboratory required.
Send resume to HR, Swabplus, LP. 9669 Hermosa Ave, Rancho Cucamonga, CA 91730