Master of Engineering and Automation from Newcastle University, UK. After graduation, he has been engaged in the field of automation engineering for more than 20 years, with extensive experience in the design and development of overseas pharmaceutical and chemical control systems. He has worked for Emerson in the UK, is proficient in process control for multiple industries such as biopharmaceuticals and chemical engineering, has rich experience in GMP and GAMP projects, and is familiar with international regulations such as FDA, MHRA, and EMA.
Senior expert in the field of automation, with 18 years of experience in the automation industry. He has extensive practical experience in biopharmaceutical process control, complex chemical process control, batch system design, SIS system design and application, and is proficient in the design and application of Emerson DeltaV DCS, Siemens PCS7 and S7 series PLCs, and Yokogawa Centum VP systems. He has previously worked for foreign companies such as Emerson Process Control Co., Ltd., Suwei Special Polymers Co., Ltd., and Fubao China Management Co., Ltd., leading the implementation of various large-scale automation projects.
Possesses a composite technical capability in the field of automation in the pharmaceutical industry, with unique professional advantages in non-standard automation design and computerized system validation (CSV) implementation. Skilled in completing non-standard automation production lines and specialized equipment solutions based on specific process requirements of pharmaceutical clients, covering the entire process from conceptual design, electrical control integration to software development. In terms of compliance validation, proficient in the GAMP5 validation system, with complete experience in writing and executing validation protocols, covering all stages of DQ/IQ/OQ/PQ as well as key aspects such as risk assessment and traceability matrices. Deeply engaged in the pharmaceutical industry, familiar with the automation control requirements of typical processes in both API and formulation segments, capable of integrating compliance requirements into solution design, balancing technical advancement, regulatory compliance, and engineering feasibility, providing clients with reliable overall automation solutions.
Graduated from a top engineering university in South Korea, currently serving as a senior process automation engineer, specializing in full lifecycle project implementation based on the S88 batch control standard. His core strength lies in preemptively integrating CSV (GAMP 5) strategies into the architecture design phase, effectively mitigating project compliance risks. Proficient in both Siemens PCS 7 and Emerson DeltaV DCS platforms, he possesses comprehensive capabilities in industrial control network topology planning and system configuration. Additionally, he has extensive on-site experience, covering hardware and software installation guidance, loop testing, and communication troubleshooting, adept at translating design logic into stable and reliable production systems.
Focused on Siemens PCS7 process control system and WinCC human-machine interface development, with full-process project implementation experience in the biopharmaceutical GMP environment. Completed computerized system validation (CSV) based on the GAMP5 V-model, proficient in ISA-88 batch control configuration standards, familiar with PRP/MRP industrial ring redundancy architecture and mainstream industrial protocols such as PROFINET, OPC UA, and Modbus TCP. Committed to delivering safe, reliable, and traceable pharmaceutical automation solutions for clients within a compliant framework. Familiar with GMP regulatory requirements in the pharmaceutical industry, with full-process project delivery capabilities from requirements analysis, system design, configuration programming to on-site commissioning. In terms of computerized system validation, strictly follows the GAMP5 V-model framework, leading the formulation and execution of validation plans (IQ/OQ/PQ) to ensure that the system meets data integrity and audit trail requirements.
With years of experience in the chemical and pharmaceutical industries, he is proficient in fine chemical and biopharmaceutical production processes, adept at translating complex process requirements into practical automation solutions. He is skilled in using both Emerson DeltaV and Siemens PCS7 platforms for system configuration development, implementing Batch projects based on the ISA-88 batch control standard, and has accumulated extensive hands-on experience in recipe management, batch division, and modular programming of unit equipment. He also possesses the overall design capability for non-standard production line automation solutions, capable of independently completing the entire process from solution planning, configuration programming, on-site commissioning to acceptance delivery. He is committed to providing clients with efficient, compliant, and traceable process automation services through cross-platform technical capabilities and solid engineering experience.