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Hvac lead

Jll
Hvac
Posted: 14h ago
Offer description

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 Description
Perform 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 Responsibilities
Team Leadership & Compliance:
Manage a team of HVAC technicians while following JLL guidelines and pharmaceutical client quality standards
Ensure all work complies with FDA regulations, Good Manufacturing Practices (GMP), and pharmaceutical industry standards
Maintain detailed documentation and validation records for all HVAC system modifications and maintenance
Critical Systems Management:
Assist the Building Lead in overseeing cleanroom HVAC systems, including HEPA/ULPA filtration systems, laminar airflow units, and biosafety cabinets
Monitor 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 environments
Monitor specialized equipment including isolators, containment systems, and controlled atmosphere storage areas
Preventive Maintenance & Validation:
Perform preventive maintenance on all critical pharmaceutical manufacturing support systems following validated procedures
Execute Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols
Maintain cleanroom integrity during all maintenance activities, including proper gowning procedures and contamination control
Complete comprehensive documentation including calibration records, maintenance logs, and deviation reports
Ensure minimal disruption to manufacturing operations through scheduled maintenance windows
Quality & Regulatory Compliance:
Maintain pharmaceutical-grade environmental controls in compliance with USP standards
Perform system monitoring and data logging for regulatory submissions and audits
Handle controlled substances and hazardous materials according to pharmaceutical safety protocols
Support validation activities and regulatory inspections as required
Qualifications
Education & Certification:
High school diploma or equivalent required
Completion of apprentice program plus minimum two years of related trade schooling or military experience
Universal CFC recovery certification required
Additional pharmaceutical-specific requirements: Cleanroom certification and GMP training preferred
Experience:
Minimum four (4) years' experience in commercial HVAC/refrigeration trade
Pharmaceutical manufacturing experience strongly preferred
Experience with cleanroom environments, HEPA filtration systems, and critical environmental controls
Knowledge of pharmaceutical validation processes and regulatory requirements
Special Knowledge & Skills:
Skilled in specialized pharmaceutical HVAC equipment including biosafety cabinets, laminar flow units, and containment systems
Knowledge of OSHA standards, city codes, and FDA regulations pertaining to pharmaceutical manufacturing environments
Understanding of USP standards for environmental monitoring and control
Familiarity with 21 CFR Part 11 for electronic records and signatures
Proficient with computerized maintenance management systems (CMMS) and building automation systems
Personal Characteristics:
Team player with strong attention to detail required for pharmaceutical quality standards
Excellent interpersonal skills and ability to communicate effectively in oral and written reports
Ability to work in highly regulated environment with strict documentation requirements
Computer proficiency including pharmaceutical-specific software systems
Physical Requirements
The 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 effectively
Frequently walk, reach, and perform physical tasks in confined spaces
Lift and move up to 50 pounds regularly, occasionally up to 100 pounds
Specific vision abilities including close vision, color vision, and depth perception critical for precision work
Environmental Conditions:
Regular exposure to controlled pharmaceutical manufacturing environments
Work with specialized air handling equipment and high-efficiency filtration systems
Potential exposure to pharmaceutical compounds requiring appropriate PPE
On-call duties and overtime as required for critical manufacturing support
Must complete enhanced background screening and drug/alcohol testing for pharmaceutical facility access
Location:
On-site –Cork, IRL
If this job description resonates with you, we encourage you to apply even if you don't meet all of the requirements.
We're interested in getting to know you and what you bring to the table
JLL Privacy Notice
Jones Lang LaSalle (JLL), together with its subsidiaries and affiliates, is a leading global provider of real estate and investment management services.
We take our responsibility to protect the personal information provided to us seriously.
Generally the personal information we collect from you are for the purposes of processing in connection with JLL's recruitment process.
We endeavour to keep your personal information secure with appropriate level of security and keep for as long as we need it for legitimate business or legal reasons.
We will then delete it safely and securely.
For more information about how JLL processes your personal data, please view our Candidate Privacy Statement.
For additional details please see our career site pages for each country.
For candidates in the United States, please see a full copy of our Equal Employment Opportunity policy here.
Jones Lang LaSalle ("JLL") is an Equal Opportunity Employer and is committed to working with and providing reasonable accommodations to individuals with disabilities.
If you need a reasonable accommodation because of a disability for any part of the employment process – including the online application and/or overall selection process – you may email us at This email is only to request an accommodation.
Please direct any other general recruiting inquiries to our Contact Us page > I want to work for JLL.

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