Marko Pavlovic

Leading a site-wide reconstruction project in a GMP-regulated pharmaceutical environment Coordinating engineering, production, QA, and external contractors across multiple systems and production areas Acting as the interface between construction activities and operational readiness Ensuring GMP-compliant implementation of new systems, utilities, and production lines Managing equipment installation, qualification, and commissioning (IQ/OQ/PQ) Driving cross-functional alignment to ensure project timelines and production continuity

Led engineering and CAPEX projects including equipment design, installation, and qualification Developed and executed URS, FAT, SAT, and IQ/OQ/PQ documentation Optimized pharmaceutical production processes in GMP environments Supported technology transfer and process scale-up activities Collaborated with QA, production, and maintenance teams to ensure compliance and efficiency

Established technical cleanliness standards for next-generation lithium-ion battery manufacturing Designed and implemented contamination control strategies in accordance with VDA 19 and ISO 14644 Developed plant-wide cleanliness protocols and SOPs Improved contamination control efficiency through implementation of particle control strategies Led audits and validation of cleanliness monitoring systems Trained engineering and production teams on contamination control standards Collaborated cross-functionally to reduce contamination risks across manufacturing processes