Laboratory Resource Management System Administrator

Responsibilities Maintain and update LRMS master data (employees, competencies, instruments, test steps). Configure scheduling parameters, competency matrices, and priority rankings. Manage user accounts, permissions, and roles within the LRMS. Oversee scheduling of stability pulls, test steps, and batched testing per SOP requirements. Ensure accurate assignment of analysts based on competencies and availability. Validate data uploads and resolve discrepancies in employee, instrument, and test configurations. Address system errors (e.g., negative hours, notification failures) and escalate complex issues. Provide guidance on scheduling functionality and impact of changes on testing timelines. Qualifications Bachelor’s degree in Life Sciences, IT, or related field with a minimum of 5 years of experience (laboratory/pharmaceutical experience preferred) Strong understanding of GMP requirements and SOP compliance. Proficiency in data management and troubleshooting. Excellent communication and problem-solving skills. Mathematical and scientific reasoning ability. Ability to learn and retain technical information. Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form. Well organized with ability to multitask; strategy is focused on personal time management and efficiency. Shift: Monday-Friday 8am-5pm. 100% on-site. Equal Opportunity Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by emailing View email address on click.appcast.io with the job number, title, and location. Notice to Agency and Search Firm Representatives: Catalent is not accepting unsolicited resumes from agencies or search firms for this job posting. #J-18808-Ljbffr Catalent