Process Engineer

Works independently under close supervision, responsible for all phases of small-scale assigned process improvement projects, ensuring the successful conclusion of all phases within an appropriate time and at appropriate cost. Assist in feasibility studies and implementing process improvement. Create necessary documentation and aides in communication to personnel. NuSil (apart of Avantor) is seeking a Process Engineer III to be responsible for all phases of silicone products manufacturing process improvement projects, ensuring the successful conclusion of all phases within designated time and deliverables. The Process Engineer III implements process improvements to meet quality standards, performs feasibility studies, solves problems, and creates necessary documentation in Agile and SAP environments and they aide in communication to personnel. This is a full-time position in person based out of our Carpinteria, CA office. How you will thrive and create an impact: Provides technical process ownership to core manufacturing processes, further improves and develops process methods, systems, and support infrastructure to optimize production rates, efficiencies, yields, costs and quality performance. Supports manufacturing department and SAP operations by creating master recipes, issues quality notifications, processes non conformances Analyses manufacturing, product, and process data to improve products and to monitor processes Participates KAIZEN events, conducts Gemba walks, 5S’s, R3’s or PSSR’s. Ensuring planned engineering (process) progress with respect to the process engineering deliverables, process engineering planning & scheduling, preparation of progress reports, utilization of resources effectively & efficiently. Provides operational leadership by managing design calculations, Process Optimization, sizing & selection of equipment etc. Review of specifications, datasheets, installation, start-up and validation of new or improved process equipment and technologies. Interacts with customers, internal team members and vendors to develop process and equipment specifications. Prepares qualification reports, flow diagrams, and charts on research data and information. Implements and maintains appropriate engineering records consistent with cGMP and ISO regulations for production of Life Science biochemicals and reagents. Work closely with engineers/production staff. quality staff to monitor and improve the efficiency, output and safety of the plant Analyze downtime to identify chronic/sporadic failures and lead reliability improvement efforts. Making observations and taking measurements directly, as well as collecting and interpreting data from the other technical and operating staff involved. Lead RCA (Root Cause Analysis) and performs PFMEA’s of processes to identify root cause and implement corrective actions to prevent recurrence ensuring that all aspects of an operation or process meet specified regulations. Development and utilization of key reliability metrics to consistently measure performance. Support manufacturing and maintenance efforts as needed by the operation. Manage multiple projects as deemed necessary based on requirements. Develop new manufacturing processes and assess the adequacy of equipment to meet ever changing market/manufacturing demands. Identifies new equipment and technologies to support continuous improvement and capacity expansion of core capabilities. Design, validate and commission new production equipment and tooling, monitor modifications and upgrades, and troubleshoot existing processes . Develops project budgets associated with the procurement of new equipment and technologies . Performs other duties as assigned.

Education: Bachelor’s degree in Chemistry, Chemical Engineering or related field.

Minimum of 7-10 years of working experience in a manufacturing environment, in an engineering capacity involving