
End-to-end commissioning and qualification of new pharma manufacturing facilities, from utilities to OSD production lines.
IQ/OQ protocol review and execution for bioreactors, autoclaves, isolators, freeze dryers, and centrifuges.
Commissioning of WFI, Purified Water, Clean Steam, HVAC, Compressed Air, and Chilled Water systems.
Contractor coordination, scheduling, HSE supervision, and progress tracking on pharma construction projects.
CTOP, VTOP, and TOS documentation review, walkdowns, and Mechanical Completion package coordination.
Supplier audits, incoming material QC, and piping documentation review (WPS, WPQR, pressure tests, orbital welding).