Jobs 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.

Lead CQV activities for GMP-regulated pharmaceutical and biotech capital projects. Develop CQV strategies, manage schedules/budgets/resources, oversee FAT/SAT and IQ/OQ/PQ, ensure cGMP/FDA/GAMP/ISPE compliance, coordinate cross-functional teams and vendors, support startup/tech transfer, and report project KPIs to leadership.

Lead commissioning, qualification and start-up activities for pharmaceutical/biopharmaceutical process equipment, utilities and facilities. Develop and execute validation deliverables (DQ, FAT, SAT, IQ/OQ/PQ), perform field testing, support Project Validation Plans, mentor junior engineers, coordinate cross-functional teams, and occasionally travel for FATs or vendor meetings.

Lead commissioning, qualification and start-up of pharmaceutical/biopharmaceutical systems. Develop and execute DQ/FAT/SAT/IQ/OQ/PQ and validation plans, perform field testing, coordinate cross-functional teams and vendors, supervise contractors, mentor validation engineers, support project delivery and occasional travel.

Lead commissioning, qualification and validation of bioprocess and pharma process equipment (upstream/downstream), develop and execute qualification deliverables (FAT/SAT/IQ/OQ/PQ), prepare/execute protocols, manage deviations and reports, coordinate cross-functional teams, support client relationships and business development, occasionally travel for FATs/vendor meetings and support shutdowns/extended hours.

Lead and manage commissioning, qualification, design, and startup of biotech/pharma equipment, systems, and facilities. Oversee capital and greenfield projects from feasibility through handover, coordinate vendors and contractors, review technical documentation, integrate safety/HAZOP, support automation sequencing, manage project controls and cross-functional stakeholders, mentor junior staff, and travel to client sites for installation, FATs, and commissioning activities.

Lead commissioning, qualification, and start-up of bioprocess and pharmaceutical process equipment. Develop and execute qualification deliverables (VPP, RTM, DQ, FAT/SAT, IQ/OQ/PQ), prepare and execute protocols, resolve deviations, summarize data, manage client relationships, lead engineers, coordinate cross-functional teams, support business development, and provide occasional on-site travel and extended hours during installations and validations.

Lead commissioning, qualification, and start-up activities for pharmaceutical/biopharmaceutical equipment, systems, and facilities. Develop and execute DQ/FAT/SAT/IQ/OQ/PQ and related validation deliverables, perform field testing, support project validation plans, coordinate cross-functional teams, supervise contractors, and support client management, scheduling, and occasional vendor/FAT travel.

Lead commissioning, qualification and start-up activities for bioprocess and process equipment. Develop and execute qualification deliverables and protocols (FAT/SAT/IQ/OQ/PQ), summarize data, resolve deviations, and prepare reports. Coordinate cross-functional teams, manage client relationships, support project scheduling/budgeting and business development, and oversee site work including installations and safety compliance. Occasional travel and extended hours during commissioning/shutdowns.

Lead commissioning, qualification and start-up of pharmaceutical/biopharmaceutical cGMP process equipment, utilities and facilities. Develop and execute qualification deliverables (DQ, FAT, SAT, IQ, OQ, PQ), perform field testing, support validation plans, coordinate cross-functional teams, mentor junior engineers, supervise contractors, and support client relations and business development. Work is on client sites in the Carlsbad area with occasional travel and possible extended hours during critical phases.

Lead commissioning, qualification and validation of pharmaceutical/biotech process equipment, utilities and facilities. Develop and execute DQ/FAT/SAT/IQ/OQ/PQ, field-test protocols, validation plans, supervise contractors, mentor validation engineers, and support project delivery and client relationships on-site.