SR Process Engineer

CAI is a 100% employee-owned company established in 1996, that has grown year over year to almost 750 people worldwide. We provide commissioning, qualification, validation, start-up, project management and other consulting services to mission critical industries. We are global partner in providing professional services to enhance operational performance and reliability. We deliver consistently, Expertly, and Completely. The Role

In this role, you will be responsible for ensuring operability and reliability of equipment. This role is highly execution-focused and requires regular on-the-floor presence to support manufacturing operations, troubleshoot equipment issues in real time, and directly support technicians and operators as needed. You will work closely with Manufacturing, Process Development, and iPark End Users to investigate, troubleshoot, and repair issues related to process equipment. You will monitor process performance and recommend/implement equipment related process and continuous improvement projects. We expect you to enjoy working in a fast-paced, dynamic, and innovative environment. Employee Type: Full Time Employee

Work location: Fujisawa, Kanagawa, Japan

Responsibilities

Provide direct engineering support and subject matter expertise for equipment including Ultrafiltration, Chromatography, Single Use Mixers, Temperature Control Units, Fermenters, Reaction Vessels, Microfluidizers, Analytical Equipment, Component Prep Equipment, Critical Utilities, and more. Develop, deliver, and support training for manufacturing operators and technicians on equipment operation, troubleshooting, and best practices, ensuring consistent and reliable execution of Enzymatics processes. Leverage subject matter expertise to directly support execution of Manufacturing activities, including hands-on troubleshooting, equipment setup, and recovery activities when required. Reduce manufacturing events, user interventions, and batch record excursions by ensuring optimal functionality of equipment and machinery. Participate in all phases of engineering projects related to processing equipment, including design, equipment procurement, asset induction, construction, installation, start-up, commissioning, qualification, and fit-for-purpose validation of facilities and/or equipment, as applicable. Respond to alarms, Out of Specification Conditions, and Out of Tolerances and ensure product impact assessments are performed as necessary. Troubleshoot equipment to determine root cause of failure modes, independently drive failure resolution and repair, own Corrective/Preventative Actions and associated Change Controls. Support implementation of Enzymatics CMMS program to enable asset and maintenance management for all relevant equipment. Own and support maintenance and repair of Enzymatics equipment assets through CMMS (preventative maintenance plans, calibration data sheets, spare parts, work order workflows as applicable). Coordinate and support end-to-end vendor-driven repair, calibration and maintenance of equipment, where necessary. Own and support quality records (e.g., Change Controls, Deviations, CAPAs) related to Enzymatics equipment, appropriate for a non-GMP but controlled manufacturing environment. Maintain Engineering Turnover Packages, including specifications, component lists, operating manuals, and drawings for Enzymatics equipment. Meticulously document all activities related to manufacturing setup, troubleshooting, and automated method updates per applicable SOPs and guidelines. Develop and implement updates for automated methods of processing equipment, ensuring seamless integration and minimal disruption to ongoing operations. Provide guidance and training on new processes and equipment. Work closely with the Quality Assurance team to ensure all manufacturing processes meet internal and external regulatory requirements, supporting deviation initiation, CAPAs, and out-of-tolerance investigations. Ensure all manufacturing activities comply with health, safety, and environmental regulations. Perform operational assessments to ensure procedures and tools are in place. Follow all relevant ISO regulations, guidelines, and company policies to ensure compliance with regulatory and internal requirements. Execute tasks precisely as defined in internal guiding documents including but not limited to standard operating procedures (SOPs) and work instructions. Follow Good Documentation Practices and Data Integrity requirements to ensure data, documentation, and records are completed and maintained for use by the business and available to support audits or inspections. Complete training in assigned required learning plan according to the defined timing and the prescribed requalification cadence.