Hard Servies Lead

Hard Services Lead - JLL Life Sciences

Large-Scale Pharmaceutical Manufacturing Facility Ireland

Position Summary

The Hard Services Lead is a strategic mission-critical role responsible for ensuring the operational excellence and regulatory compliance of a large-scale pharmaceutical manufacturing facilitys building infrastructure. This position directly impacts the production of life-saving medications and medical devices by maintaining critical building systems cleanroom environments and controlled atmospheres that meet stringent FDA EMA and HPRA standards. As a key leader within JLL Life Sciences operations team you will drive facility uptime ensure regulatory compliance and optimize maintenance operations for one of Irelands premier pharmaceutical manufacturing sites.

Key Responsibilities

• Lead comprehensive hard services programs for pharmaceutical manufacturing facility including HVAC systems cleanroom environments controlled atmospheres and critical utility systems to ensure 99.9% uptime for production operations

• Develop implement and continuously optimize preventive maintenance strategies using risk-based methodologies ensuring all building systems support GMP/GDP compliance and minimize unplanned downtime that could impact drug production

• Manage emergency response protocols for critical building system failures coordinating rapid resolution of issues affecting cleanroom classifications environmental controls and manufacturing-critical infrastructure with minimal production impact

• Oversee vendor management and contractor coordination for specialized pharmaceutical facility services including qualification of suppliers performance monitoring and ensuring all external maintenance activities meet life sciences regulatory requirements

• Ensure strict adherence to regulatory compliance standards (FDA EMA HPRA) through meticulous documentation validation of building system performance and maintenance of qualification status for all facility infrastructure supporting drug manufacturing

• Lead annual budget planning and cost optimization initiatives for building maintenance operations developing strategic spending plans that balance regulatory compliance operational efficiency and capital expenditure requirements while achieving cost targets

• Champion health & safety excellence by conducting comprehensive risk assessments implementing safety protocols for maintenance activities in pharmaceutical environments and ensuring team compliance with both JLL and client safety standards

• Maintain detailed documentation and reporting systems including maintenance records compliance audits system performance metrics and regulatory inspection readiness documentation to support FDA/EMA inspections and internal quality reviews

• Collaborate cross-functionally with Production Quality Assurance Engineering and Regulatory Affairs teams to align building maintenance activities with manufacturing schedules and regulatory requirements

• Lead and develop a high-performing maintenance team through coaching training and performance management while fostering a culture of continuous improvement and regulatory excellence

• Manage capital improvement projects for building infrastructure upgrades ensuring projects meet pharmaceutical design standards regulatory requirements and are delivered on time and within budget

• Conduct regular facility condition assessments and develop long-term building maintenance strategies that anticipate equipment lifecycle needs and support facility expansion or modernization plans

Essential Qualifications

Education:

• Bachelors degree in Mechanical Engineering Electrical Engineering Facilities Management or related technical discipline

• Experience:

• Minimum 7-10 years of building maintenance experience in pharmaceutical biotechnology or medical device manufacturing environments

• 5 years of leadership experience managing maintenance teams in regulated life sciences facilities

• Proven track record supporting FDA EMA or HPRA regulatory inspections and compliance audits

Regulatory & Industry Knowledge:

• Deep understanding of Irish building regulations EU pharmaceutical regulations and international GMP/GDP standards

• Experience with cleanroom classifications (ISO 14644) controlled environments and critical utility systems

• Knowledge of ISPE (International Society for Pharmaceutical Engineering) guidelines and industry best practices

Certifications (Preferred):

• Certified Maintenance & Reliability Professional (CMRP)

• Project Management Professional (PMP) or equivalent

• Irish Safe Pass certification

• HVAC/refrigeration technician certifications

Technical Skills

• Building Systems Expertise:

• Advanced knowledge of pharmaceutical-grade HVAC systems including air handling units cleanroom pressurization temperature/humidity control and filtration systems

• Electrical systems management including emergency power UPS systems critical power distribution and energy management

• Plumbing and process utilities including purified water systems compressed air steam and waste management systems

• Fire safety and life protection systems specific to pharmaceutical manufacturing environments

• Technology & Software:

• Proficiency with CMMS (Computerized Maintenance Management Systems) such as Maximo SAP PM or similar platforms

• Building automation systems (BAS) and building management systems (BMS) operation and troubleshooting

• Microsoft Office Suite project management software and data analysis tools

• CAD software for facility drawings and maintenance documentation

Project Management:

• Experience managing complex maintenance projects from planning through execution

• Budget management and financial analysis capabilities

• Change management and process improvement methodologies

• Vendor negotiation and contract management skills

Essential Soft Skills

Leadership Excellence:

• Proven ability to lead motivate and develop cross-functional maintenance teams in fast-paced pharmaceutical environments

• Strong coaching and mentoring skills with focus on building technical capabilities and regulatory awareness

Communication & Collaboration:

• Exceptional verbal and written communication skills with ability to present complex technical information to diverse stakeholders

• Experience interfacing with senior leadership regulatory agencies and external auditors

• Collaborative approach to working with Production Quality Engineering and external vendor teams

Problem-Solving & Decision-Making:

• Strong analytical and critical thinking skills with ability to troubleshoot complex building system issues under pressure

• Data-driven decision-making approach with focus on root cause analysis and continuous improvement

• Ability to balance competing priorities while maintaining focus on patient safety and product quality

Regulatory Mindset:

• Meticulous attention to detail with understanding that maintenance activities directly impact patient safety

• Strong documentation discipline and commitment to maintaining detailed audit-ready records