Teams at Agilent Technologies

Plan, coordinate, and optimize daily, weekly, and long-term production schedules in a GMP/cGMP manufacturing environment. Collaborate with Manufacturing, QC, Engineering, and Maintenance to ensure material, equipment, and personnel availability. Monitor schedule adherence and equipment utilization, resolve conflicts, communicate changes, and support new product introductions, maintenance, and continuous improvement initiatives to meet customer and business objectives.

Support design, construction, commissioning, qualification, and turnover of capital projects for pharma/biopharma manufacturing. Manage project schedules and budgets, develop URSs, specify equipment/instrumentation, support tech transfer and scale-up, participate in FAT/SAT and IQ/OQ/PQ validation, and assist QA and EHS activities including PHA and PSMS compliance.

Responsible for GMP automation and controls for biopharma manufacturing: design, troubleshoot, and optimize PLC/DCS/SCADA/BAS systems; lead control system specs, change controls, and Part 11 compliance; support validation (FAT/SAT/IQ/OQ); and collaborate with QA, validation, process, and manufacturing teams to ensure uptime and regulatory compliance.