Key Responsibilities: Design, develop, and update required technical documentation Assist with the editing of quality documents (SOP's, guidelines, validation master plans, etc.) to ensure compliance with regulatory requirements Create Training slides and content Support Future state process mapping Organize, track and plan master data review Track and mange project specific deliverables Key Requirements and Technology Experience: Skills-Editing of quality documents (SOP's, guidelines, validation master plans, etc.) to ensure compliance with regulatory requirements. Background in digital IT or scientific fields Experience with QC (quality control) activities Experience with LIMS systems (e.g., LabVantage, iLMS, Sequel, or related systems) Experience deploying digital systems (e.g., LabWare, LIMS) strongly preferred Knowledge of validation processes is a plus Previous experience in pharmaceutical, analytical, or biotech environments (e.g., Veeva) preferred Proficiency in PowerPoint with the ability to create training materials, including slides and graphics.