JLL empowers you to shape a brighter way.Our people at JLL and JLL Technologies are shaping the future of real estate for a better world by combining world class services, advisory and technology for our clients. We are committed to hiring the best, most talented people and empowering them to thrive, grow meaningful careers and to find a place where they belong. Whether you've got deep experience in commercial real estate, skilled trades or technology, or you're looking to apply your relevant experience to a new industry, join our team as we help shape a brighter way forward.General DescriptionPerform and manage team on HVAC installation, repair, and maintenance of critical environmental control systems in pharmaceutical manufacturing facilities. Installs, repairs, and maintains HVAC operating equipment and controls essential for maintaining cleanroom environments, temperature/humidity control, and air quality standards required for pharmaceutical production. Conducts routine and ongoing assessment of building systems operations while ensuring compliance with FDA, GMP, and pharmaceutical industry regulations.Principal Job Duties and ResponsibilitiesTeam Leadership & Compliance:Manage a team of HVAC technicians while following JLL guidelines and pharmaceutical client quality standardsEnsure all work complies with FDA regulations, Good Manufacturing Practices (GMP), and pharmaceutical industry standardsMaintain detailed documentation and validation records for all HVAC system modifications and maintenanceCritical Systems Management:Assist the Building Lead in overseeing cleanroom HVAC systems, including HEPA/ULPA filtration systems, laminar airflow units, and biosafety cabinetsMonitor and maintain critical environmental parameters including temperature, humidity, differential pressure, and air changes per hour (ACH)Operate and adjust refrigeration, heat exchanger, HVAC, electrical, emergency backup systems specifically designed for pharmaceutical manufacturing environmentsMonitor specialized equipment including isolators, containment systems, and controlled atmosphere storage areasPreventive Maintenance & Validation:Perform preventive maintenance on all critical pharmaceutical manufacturing support systems following validated proceduresExecute Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocolsMaintain cleanroom integrity during all maintenance activities, including proper gowning procedures and contamination controlComplete comprehensive documentation including calibration records, maintenance logs, and deviation reportsEnsure minimal disruption to manufacturing operations through scheduled maintenance windowsQuality & Regulatory Compliance:Maintain pharmaceutical-grade environmental controls in compliance with USP standardsPerform system monitoring and data logging for regulatory submissions and auditsHandle controlled substances and hazardous materials according to pharmaceutical safety protocolsSupport validation activities and regulatory inspections as requiredQualificationsEducation & Certification:High school diploma or equivalent requiredCompletion of apprentice program plus minimum two years of related trade schooling or military experienceUniversal CFC recovery certification requiredAdditional pharmaceutical-specific requirements: Cleanroom certification and GMP training preferredExperience:Minimum four (4) years' experience in commercial HVAC/refrigeration tradePharmaceutical manufacturing experience strongly preferredExperience with cleanroom environments, HEPA filtration systems, and critical environmental controlsKnowledge of pharmaceutical validation processes and regulatory requirementsSpecial Knowledge & Skills:Skilled in specialized pharmaceutical HVAC equipment including biosafety cabinets, laminar flow units, and containment systemsKnowledge of OSHA standards, city codes, and FDA regulations pertaining to pharmaceutical manufacturing environmentsUnderstanding of USP standards for environmental monitoring and controlFamiliarity with 21 CFR Part 11 for electronic records and signaturesProficient with computerized maintenance management systems (CMMS) and building automation systemsPersonal Characteristics:Team player with strong attention to detail required for pharmaceutical quality standardsExcellent interpersonal skills and ability to communicate effectively in oral and written reportsAbility to work in highly regulated environment with strict documentation requirementsComputer proficiency including pharmaceutical-specific software systemsPhysical RequirementsThe physical demands are representative of pharmaceutical manufacturing environments where employees must successfully perform essential functions while maintaining cleanroom protocols(Source: Lead HVAC ).Standard Physical Requirements:Regularly required to stand, use hands for detailed work, and communicate effectivelyFrequently walk, reach, and perform physical tasks in confined spacesLift and move up to 50 pounds regularly, occasionally up to 100 poundsSpecific vision abilities including close vision, color vision, and depth perception critical for precision workEnvironmental Conditions:Regular exposure to controlled pharmaceutical manufacturing environmentsWork with specialized air handling equipment and high-efficiency filtration systemsPotential exposure to pharmaceutical compounds requiring appropriate PPEOn-call duties and overtime as required for critical manufacturing supportMust complete enhanced background screening and drug/alcohol testing for pharmaceutical facility accessLocation:On-site –Cork, IRLIf this job description resonates with you, we encourage you to apply even if you don't meet all of the requirements. 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