Mechanical Engineer

Mechanical Engineer (Facilities & Utilities) – Pharmaceutical ManufacturingLocation: Andover, MAEmployment Type: Full-TimeExperience Level: 4–9 YearsPosition SummaryWe are seeking a Mechanical Engineer with 4–9 years of experience to support the design, execution, and commissioning of facility and utility systems for a pharmaceutical manufacturing project in Andover, MA. The successful candidate will be responsible for the engineering and lifecycle management of critical facility infrastructure including HVAC systems, chillers, boilers, steam systems, compressed air, and related mechanical utilities that support GMP manufacturing operations.The ideal candidate will possess a strong background in industrial or pharmaceutical facility engineering, utility systems, and multidisciplinary project execution. Experience working within regulated manufacturing environments is highly desirable.Key ResponsibilitiesSupport the design, specification, and implementation of mechanical facility and utility systems for pharmaceutical manufacturing operations.Develop engineering deliverables including equipment specifications, calculations, system assessments, P&IDs, and design packages.Provide technical oversight for HVAC systems, chilled water systems, boilers, steam distribution, condensate return, compressed air systems, and other plant utilities.Coordinate with architectural, process, electrical, controls, and validation teams throughout project execution.Review vendor submittals, equipment selections, and contractor deliverables to ensure compliance with project requirements and industry standards.Participate in facility assessments, troubleshooting activities, and root cause investigations related to mechanical equipment and utility systems.Support installation, commissioning, startup, and qualification activities for facility infrastructure systems.Ensure designs comply with applicable codes, industry standards, GMP requirements, and company engineering practices.Assist in project planning, scheduling, cost estimating, and risk management activities.Support management of change (MOC), deviation investigations, and CAPA activities as required.Interface with operations, maintenance, quality, and external engineering partners to ensure successful project delivery.Required QualificationsBachelor's degree in Mechanical Engineering or related engineering discipline.4–9 years of mechanical engineering experience in pharmaceutical, biotechnology, life sciences, industrial manufacturing, or similar regulated environments.Experience with facility utility systems including:HVAC systemsChilled water systemsBoilers and steam systemsCooling towersCompressed air systemsBuilding mechanical infrastructureKnowledge of engineering design principles, equipment specifications, and construction support activities.Familiarity with applicable codes and standards including ASHRAE, ASME, and applicable building codes.Strong technical problem-solving and troubleshooting skills.Excellent communication and coordination skills with cross-functional project teams.Preferred QualificationsExperience supporting GMP pharmaceutical or biotechnology manufacturing facilities.Experience with cleanroom HVAC systems and environmental control requirements.Knowledge of commissioning, qualification, and validation processes.Understanding of FDA-regulated environments and industry best practices.Experience supporting capital projects from conceptual design through startup.Professional Engineer (PE) license or Engineer-in-Training (EIT) certification is a plus.Key CompetenciesMechanical Utilities EngineeringHVAC Design & OptimizationFacility Infrastructure SystemsPharmaceutical Manufacturing FacilitiesProject EngineeringEquipment Specification & ProcurementCommissioning & StartupCross-Functional CollaborationTechnical DocumentationRoot Cause Analysis & Troubleshooting