Cqv Engineer - HVAC (Life Science & Pharmaceutical) #Rt

Your new company Client is an expert in automation and digital systems for pharmaceutical and biotech manufacturing, seeking to hire a yearly contract renewable CQV Engineer. Duration : Yearly Contract Salary : open for negotiation Your new role We are seeking an experienced CQV Engineer with experience in HVAC, you will play a critical role in executing commissioning, qualification, and validation of HVAC systems. Develop, review, and execute qualification documentation for HVAC and cleanroom systems, including IQ, OQ, PQ, requalification protocols, deviation records, and summary reports. Conduct qualification activities for AHUs, HVAC systems, ductwork, environmental control systems, HEPA filtration units, temperature and humidity controls, differential pressure systems, and Grade C/D cleanrooms. Plan, coordinate, and assess cleanroom certification activities, including smoke studies, airflow and velocity measurements, air change rate calculations, HEPA integrity testing, non-viable particle monitoring, pressure cascade verification, and environmental mapping. Support FAT, SAT, commissioning, start-up, system balancing, punch-list resolution, and final handover activities. Review and verify vendor and contractor deliverables, including test reports, calibration certificates, quality records, and turnover documentation. Manage and close qualification-related deviations, change controls, risk assessments, action items, and punch-list activities. Collaborate with Quality, Engineering, Facilities, Automation, Operations, Validation teams, and external contractors to ensure successful project execution and milestone achievement. Support the verification of HVAC automation controls and EMS/BMS monitoring systems where these form part of the validated system scope. Ensure all qualification documentation is accurate, complete, audit-ready, and maintained in compliance with GMP requirements and Good Documentation Practices (GDP). What you'll need to succeed Bachelor’s degree in Mechanical Engineering, Chemical Engineering, Building Services, or a related discipline. Minimum 3 years of HVAC and cleanroom CQV experience within pharmaceutical or biotechnology facilities. Strong knowledge of EU GMP Annex 1, ISO 14644 cleanroom standards, ISPE Baseline Guides, and Good Documentation Practices. Hands-on experience with cleanroom qualification testing, HVAC control verification, deviations, and qualification reporting. What you'll get in return This is an exciting opportunity to contribute to large scale pharmaceutical projects. What you need to do now If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call Rachel at Hays on +65 6027 1923 or email Rachel.Tang@hays.com.sg for a confidential discussion. Referrals are welcome. Registration ID No. R24121588| EA License number: 07C3924 | Company Registration No. 200609504D