2026 Co-Op, Drug Product Automation, Visual Inspection

Support automated and semi-automated Koerber AVI systems (Switch 350, De.Sy.Re).,Assist with system configuration, troubleshooting, and operational support.,Review and analyze inspection results, defect classifications, and performance trends.,Support data reviews related to VI performance across global manufacturing sites.,Assist with documentation to support commissioning, qualification, and validation activities.,Support integration of VI systems into manufacturing networks.,Assist with IP configuration, network connectivity, and system communication troubleshooting.,Support SCADA integration and data exchange with site automation systems.,Assist in aligning vendor systems with internal automation and data standards.,Participate in cross-functional discussions with Manufacturing, IT, Quality, and vendors.,Review and analyze inspection data from global manufacturing sites (including Australia).,Identify trends, data gaps, and opportunities for standardization or improvement.,Assist in organizing and presenting data for engineering and operational review.,Support efforts to improve data accessibility and usability for manufacturing teams.

Currently pursuing a Bachelor’s or Master’s degree in Electrical, Automation, Mechanical, Computer, or Industrial Engineering, Computer Science or a related technical field.,Strong interest in automation, manufacturing systems, or industrial technology.,Comfortable working with technical systems and structured data.,Strong analytical and problem-solving skills.,Able to communicate technical concepts clearly and professionally.,Curious, self-driven, and eager to learn in a regulated manufacturing environment.,Exposure to manufacturing automation, machine vision, or industrial systems (Preferred).,Interest in pharmaceutical or regulated manufacturing environments (Preferred).,Experience working on technical projects involving hardware and software integration (Preferred).

Currently pursuing Bachelor's or Master's Degree

Site-based, requiring full-time presence at Moderna’s site.,Not eligible for remote work.,Candidates must already hold work authorization in US and be able to maintain that status without the need for future sponsorship.,Employment is contingent upon the applicant’s ability to access export-controlled information in accordance with U.S. law.,Only individuals who qualify as U.S. persons (citizens, permanent residents, asylees, or refugees) are eligible for this position.,Moderna is unable to sponsor non-U.S. persons to apply for an export control license for this role.