Teams at MMR Group

Lead CQV and project management activities for biopharma facility upgrades, Greenfield and capital projects. Oversee feasibility, design, procurement, construction, commissioning, qualification, vendor management, safety integration, and cross-functional coordination to deliver cGMP-compliant systems and facilities.

Lead and manage CQV, commissioning, qualification and project execution for pharmaceutical/biotech equipment, systems and facilities from feasibility through handover. Oversee design review, procurement, construction, vendor management, P&ID review, safety/HAZOP integration, automation sequences, FATs, and cross-functional coordination. Work onsite at client facility in Raleigh, NC; supervise contractors and support start-up, validation, and occasional extended hours or shutdown activities.

Lead commissioning, qualification and start-up of pharmaceutical and biopharmaceutical cGMP process equipment, utilities and facilities. Develop and execute qualification deliverables (DQ/FAT/SAT/IQ/OQ/PQ), perform field execution of test protocols, mentor validation engineers, coordinate cross-functional stakeholders, and support project delivery and client relations.