About the role
AI summarisedLead end-to-end commissioning activities for Building Management Systems (BMS) across GMP and non-GMP areas, ensuring compliance with stringent life sciences standards while driving system integration and successful handover to operations.
IndustrialOnsiteCustomer Projects & Services
Key Responsibilities
- Lead end-to-end commissioning activities for BMS across GMP and non-GMP areas.
- Develop and execute Commissioning Plans, IQ/OQ protocols, and traceability matrices.
- Ensure correct integration of HVAC, utilities, cleanrooms, and process support systems into BMS.
- Coordinate functional testing, alarm verification, trend validation, and system performance testing.
- Support Site Acceptance Testing (SAT) and successful system handover to operations.
- Review and approve validation documentation, deviation reports, and change controls.
- Act as primary technical interface between BMS vendors, system integrators, and project teams.
- Provide commissioning input during design stages to reduce rework and validation risk.
- Lead investigations into BMS & EMS deviations, failures, or performance issues.
Requirements
- Bachelor’s Degree in Mechanical, Electrical, or an equivalent engineering discipline.
- 7–12 years of experience in BMS, HVAC automation, or facilities systems.
- Minimum 3–5 years in pharmaceutical, biotech, or regulated life-sciences environments.
- Proven experience leading CSV, GAMP 5, and validation lifecycle management on Greenfield pharmaceutical facilities or major expansions.
- Knowledge of 21 CFR Part 11, Annex 11, and data integrity expectations.
- Familiarity with HVAC systems: AHUs, VAVs, pressure cascades, temperature & humidity control.
- Understanding of networks, servers, cybersecurity concepts related to OT systems.