An exciting opportunity for a HVAC Engineer to join a global Company at the top of their industry. Working within a high-performing site engineering team, you will focus on the technical delivery, commissioning, and qualification of critical HVAC systems.
Key Responsibilities
Lead end-to-end HVAC engineering, design review, and commissioning activities associated with site capacity expansion projects.
Draft, execute, and govern HVAC qualification protocols (FAT, SAT, IQ, OQ, PQ) in strict alignment with FDA, EMA, and ISO cleanroom standards.
Ensure peak system performance and strict parameter control (temperature, relative humidity, differential pressure, and air change rates) across expanded cleanroom suites.
Manage equipment vendors, technical sub-contractors, and engineering consultants to ensure technical submittals, URS, and design documentation meet site specs.
Partner closely with QA, Validation, Manufacturing, and EHS teams to perform root cause analyses (RCA), manage site change controls, and resolve complex technical deviations.
Qualifications & Experience
Third-level degree (BSc/BEng) in Mechanical, Building Services, or Chemical Engineering.
4+ years of dedicated HVAC engineering experience within a regulated Biopharmaceutical or Pharmaceutical manufacturing environment.
Proven background supporting capital projects, facility expansions, or commissioning & qualification (C&Q) of complex air handling systems (AHUs, exhaust fans, cleanroom air distribution).
Deep working knowledge of cGMP regulations, cleanroom classifications (ISO classes), HVAC design principles, and CMMS platforms (e.g., Maximo).
Strong analytical troubleshooting abilities, project execution focus, and clear communication skills to effectively collaborate across cross-functional site departments
