Inteldot has over 15 years in the life science industry with allocations a cross Puerto Rico, United Sates, Europe and Japan. This is a great opportunity for one of our leading clients in Puerto Rico. Administrative Shift Location: Manatí, Puerto Rico Work Arrangement: Primarily Onsite Industry: Pharmaceutical / Life Sciences Manufacturing About the Role We are seeking an experienced Senior Program/Project Manager to lead two major initiatives at a pharmaceutical manufacturing facility in Manatí, Puerto Rico: Site Master Planning (SMP) Program and Cogeneration / Combined Heat & Power (CHP) Project. This is a highly visible leadership position for an experienced capital-project professional who can independently manage schedule, budget, risk, engineering, procurement, permitting, construction, commissioning, and stakeholder coordination across both initiatives. The selected individual will serve as the single accountable Program/Project Manager and primary point of contact for both workstreams. What You’ll Do • Lead the overall planning and execution of the Site Master Planning and CHP initiatives. • Develop and maintain integrated project schedules, budgets, forecasts, milestones, and risk registers. • Coordinate Engineering, Operations, Quality, EHS, Facilities, Finance, Procurement, and Corporate Engineering/EHS stakeholders. • Lead coordination with A/E firms, contractors, equipment vendors, consultants, and other external partners. • Support Capital Appropriation Requests (CARs), cost estimating, budget tracking, and financial reporting. • Facilitate site master planning workshops and develop long-term facility expansion and capital investment strategies. • Coordinate evaluation of facility layout, production flow, space utilization, utilities, infrastructure capacity, and future expansion needs. • Lead the development of a 10+ year Site Master Plan and phased capital roadmap. • Manage the CHP feasibility study, technology/vendor selection, business case, and implementation strategy. • Coordinate CHP engineering design, utility integration, PREPA interconnection, permitting, procurement, construction, commissioning, and startup. • Manage project risks, change control, documentation, decision logs, and action tracking. • Provide weekly/monthly project updates to site and corporate leadership. • Support GMP compliance, commissioning, qualification, validation, and operational handoff activities. • Proactively identify and resolve conflicts between SMP and CHP activities, including shared engineering resources, utility tie-ins, site access, and outage windows. • Maintain a strong onsite presence and working level understanding of both initiatives throughout the engagement. Requirements: • Bachelor's degree in engineering, Construction Management, Project Management, or a related technical field. • Significant project/program management experience in pharmaceutical, biotechnology, life sciences, or other regulated manufacturing environments. • Demonstrated experience managing capital projects from planning through construction, commissioning, and closeout. • Direct experience leading site master planning or major facility planning initiatives. • Direct experience with cogeneration/CHP, power generation, or major industrial utility projects. • Experience managing engineering/design firms, contractors, vendors, and multidisciplinary teams. • Strong experience with project schedules, budgets, cost controls, risk management, and change control. • Experience working in GMP/cGMP environments. • Ability to independently manage multiple technically interdependent workstreams. • Strong written and verbal communication skills. • Ability to work onsite in Manatí, Puerto Rico on a recurring basis. Preferred Qualifications: • PMP, CCM, PE, or equivalent professional certification. • Previous experience in Puerto Rico pharmaceutical manufacturing. • Familiarity with PREPA utility interconnection requirements and EQB/environmental permitting. • Experience with CHP integration involving electrical, steam, hot-water, HVAC, or other critical utilities. • Experience with commissioning, qualification, validation, and GMP utility requirements. • Experience developing long-range capital plans for pharmaceutical or life-sciences campuses. • Experience working directly with corporate/global engineering organizations. • Bilingual English/Spanish.