Project Scheduler

*Company Description* LoopTech LLC is a cutting‑edge engineering and technology company delivering integrated Engineering, Automation, IT, and Consulting solutions that help organizations operate smarter, reduce risk, boost reliability, and make high‑impact investment decisions with confidence. We turn technical complexity into clarity, and clarity into performance. *Key Responsibilities* * Develop, maintain, and baseline integrated project schedules, including milestones, activities, dependencies, resources, and critical-path considerations. * Collect schedule updates from project managers and functional leads; validate inputs and incorporate approved changes. * Track milestones, dependencies, progress, and key decision dates; identify schedule risks, variances, and potential impacts. * Prepare clear schedule status reports, dashboards, and variance analyses for project and stakeholder review. * Facilitate schedule-planning and update meetings; document actions, assumptions, and agreed next steps. * Coordinate with project managers and functional leads to resolve conflicts, align workstreams, and maintain schedule integrity. * Maintain schedule documentation, including baselines, change logs, reporting records, and planning artifacts. *Qualifications & Experience* * Bachelor’s Degree in Engineering, Science, or related field. * Minimum of 5 years of experience in pharmaceutical industry, with at least 2 years of experience in commissioning, qualification, validation, CSV, or startup activities, or project management activities. * Relevant experience in project scheduling, project controls, program coordination, or a comparable planning role. * Proficiency with Microsoft Project, or comparable scheduling tools; strong Microsoft Excel skills. * Ability to interpret project plans, work breakdown structures, logic links, milestones, and interdependencies. * Strong written and verbal communication, organization, facilitation, and stakeholder-coordination skills. * Excellent attention to detail and ability to work independently while managing priorities. * Familiarity with schedule risk analysis, earned value concepts, Agile or hybrid delivery methods, and reporting/dashboard tools. *Preferred Qualifications* * Experience supporting cross-functional, multi-workstream, or enterprise-scale projects. * Relevant certification or formal training in project management, project controls, or scheduling is preferred. * Proficient in MS Office applications (Word, Excel, PowerPoint). * Bilingual: fluent in English and Spanish. * Ability to work onsite. * Proven background in pharmaceutical manufacturing; experience in sterile operations is highly desirable. * Ability to perform effectively in fast‑paced, highly regulated environments. Pay: $70,000.00 - $100,000.00 per year Work Location: In person