Job Description Summary Do you want to become a creator of the possible? For over 125 years, we have pursued our purpose by advancing the world of health™. We tirelessly commit to a promising future by developing innovative technologies, services, and solutions, helping the healthcare community improve safety and increase efficiency. It takes all of our imagination and passion at BD, from manufacturing to marketing our products, to see the impossible and find transformative solutions that turn our dreams into possibilities – for people today, tomorrow, and in the future. Be a creator of the possible with us! Join us! The process technician is responsible for providing specialized technical support in the execution of improvement, modification, and validation projects for equipment and systems within pharmaceutical plants. Their focus includes mechanical, electrical, electronic, and automation interventions (including PLC programming), ensuring compliance with regulatory requirements and quality standards applicable to the pharmaceutical industry. Job Description Functions* Execute and document mechanical, electrical, electronic, and software modifications on machinery and inspection systems. * Actively participate in the validation of new and existing equipment, including IQ/OQ/PQ, according to GMP guidelines and regulatory requirements. * Support the implementation of technological upgrades in production lines, ensuring operational continuity and improved efficiency. * Collaborate with multidisciplinary teams (production, quality, maintenance, validation) to ensure proper integration of changes into processes. * Develop and maintain up-to-date technical documentation (drawings, electrical diagrams, user manuals, validation protocols). * Perform diagnostics and troubleshooting on automated systems, proposing effective technical solutions. * Ensure compliance with industrial safety policies and environmental regulations during project execution. * Participate in internal and external audits by providing technical and documentary evidence of implemented changes. Education and experience* Engineering or related field (incomplete or completed) in Mechanical, Electronic, Mechatronics, Automation, or related. * Minimum of 3 years of experience in regulated industrial environments, preferably in the pharmaceutical or medical device industry. * Knowledge of PLC programming (Siemens, Allen-Bradley, etc.) and SCADA systems. * Familiarity with GMP, FDA, applicable NOMs, and validation processes. * Ability to interpret electrical drawings, control diagrams, and technical documentation. * Basic technical English. Required Skills Optional Skills . Primary Work Location MEX Cuautitlan Izcalli Additional Locations Work Shift