Jobs at MMR Group

Supports pharmaceutical client electrical projects from design review through procurement, construction, commissioning, startup, and closeout. Reviews engineering documents, shop drawings, technical data, and electrical systems; conducts field inspections; prepares commissioning protocols and reports; supervises contractors; coordinates cross-functional stakeholders; and provides technical guidance to junior engineers. Work occurs at client facilities and may include shutdowns, extended hours, construction-site visits, and PPE compliance.

Electrical Engineer supporting pharmaceutical and biotech facility projects from design review through procurement, construction, commissioning, startup, and closeout. Responsibilities include reviewing engineering and vendor submittals, overseeing electrical systems, conducting field inspections, preparing commissioning protocols, supervising contractors, coordinating cross-functional teams, and mentoring junior engineers. The role requires client-site work in Raleigh, North Carolina, including occasional extended hours during installation and commissioning.

Supports pharmaceutical and biotechnology facility electrical projects from design review through procurement, construction, commissioning, startup, and closeout. Reviews electrical designs, vendor submittals, drawings, and technical data for low- and medium-voltage systems. Conducts field inspections, commissioning protocols, and progress reviews; supervises contractors during critical installations; coordinates cross-functional teams; and provides technical guidance to junior engineers. Work is performed at client facilities and may include shutdowns, extended hours, PPE, and construction-site visits.

Supports pharmaceutical client electrical engineering projects from design review through procurement, construction, commissioning, startup, and closeout. Reviews drawings and submittals, conducts field walks, supervises contractors, prepares commissioning protocols, coordinates cross-functional stakeholders, and provides technical guidance to junior engineers. The role focuses on low- and medium-voltage systems, electrical equipment, and client-site project execution, including occasional shutdown or extended-hours support.

Provides electrical engineering support for pharmaceutical and biotech facility projects, including design and submittal reviews, procurement, construction oversight, commissioning, startup, validation, and closeout. Reviews low- and medium-voltage systems, supervises contractors, conducts field walks, prepares commissioning documentation, coordinates cross-functional teams, and guides junior engineers. The role is based at client facilities in Raleigh, North Carolina, and may require occasional shutdown or extended-hours support.

Supports pharmaceutical facility electrical projects from design review and procurement through construction, commissioning, startup, and closeout. Reviews engineering designs, vendor submittals, drawings, and technical data for low- and medium-voltage systems. Conducts field inspections, supervises contractors, prepares commissioning protocols and reports, coordinates cross-functional teams, and provides technical guidance to junior engineers. Work is performed at client facilities and may include shutdowns, extended hours, PPE, and compliance with site safety requirements.

Support pharmaceutical client as an electrical systems engineer: review designs and vendor submittals, oversee electrical projects end-to-end, perform field walks, supervise installations, participate in commissioning/startup and qualification, coordinate cross-functional teams, and provide technical guidance to junior engineers.

Provide electrical engineering support for pharmaceutical facility projects including review of designs/submittals, overseeing projects end-to-end, field job walks, commissioning/startup, supervision of contractors, and coordination with cross-functional teams during construction, commissioning, and validation.

Support pharmaceutical client as an electrical systems engineer: review designs/submittals, oversee electrical projects end-to-end, perform field walks, supervise installations, participate in commissioning/startup and qualification, coordinate cross-functional teams, and provide technical guidance to junior engineers while complying with client safety rules.

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 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 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 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.