Jobs at MMR Group

Coordinate onboarding for employees and contractors, including equipment, training, access requests, paperwork, and tracking. Maintain onboarding records and checklists, resolve basic access issues, answer administrative questions, and collaborate with IT, HR, training, and management. Provide general administrative support while ensuring onboarding remains accurate and on schedule.

Coordinate onboarding for employees and contractors, including equipment requests, training assignments, access provisioning, paperwork, and recordkeeping. Serve as an administrative contact, maintain onboarding trackers, resolve basic access issues, and coordinate with IT, HR, training, and management. Provide general administrative support while ensuring onboarding activities are completed accurately and on schedule.

Coordinate onboarding for employees and contractors, including equipment requests, training assignments, access provisioning, paperwork, and onboarding tracking. Serve as an administrative point of contact, maintain accurate records, resolve basic access issues, and coordinate with IT, HR, training, and management. Provide general administrative support while ensuring new team members are prepared to begin work on schedule.

Leads commissioning, qualification, and validation activities for sterile pharmaceutical filling and packaging operations. Manages CQV strategies, project plans, budgets, schedules, resources, documentation, FAT/SAT, commissioning, qualification, troubleshooting, reliability studies, optimization, and continuous improvement. Leads engineering teams and coordinates with production, packaging, vendors, cross-functional stakeholders, and senior leadership from project feasibility through handover.

Coordinates employee and contractor onboarding, including equipment, system access, training assignments, paperwork, checklists, and records. Serves as an administrative contact for new team members, resolves basic access issues, and collaborates with IT, HR, training, and management to keep onboarding on schedule. Provides general administrative support in an onsite, regulated consulting environment.

Lead commissioning, qualification, and validation activities for sterile pharmaceutical filling and packaging operations. Manage CQV strategies, project plans, budgets, schedules, resources, specifications, FAT/SAT, commissioning, qualification, troubleshooting, reliability studies, optimization, and continuous improvement. Coordinate vendors, production teams, cross-functional stakeholders, and senior leadership from feasibility through project handover. The role is based at client facilities in Portland, Oregon, with occasional travel, shutdown, and extended-hours support.

Leads commissioning, qualification, and validation activities for sterile and aseptic pharmaceutical filling and packaging operations. Manages CQV strategies, project plans, schedules, budgets, resources, specifications, vendor coordination, FAT/SAT, commissioning, qualification, troubleshooting, reliability studies, and process improvements. Coordinates cross-functional stakeholders and leads engineering teams from feasibility through project handover, with occasional shutdown and extended-hours support.

Lead commissioning, qualification, validation, design, troubleshooting, optimization, and continuous improvement for pharmaceutical filling and packaging systems in sterile/aseptic manufacturing environments. Develop requirements and specifications, coordinate vendors and cross-functional stakeholders, support FAT/SAT and commissioning activities, and lead engineers and project teams. The role is based at client facilities in Portland, Oregon, with occasional travel, shutdown, and extended-hours support.

Lead commissioning, qualification, validation, design, startup, troubleshooting, optimization, and continuous improvement for sterile pharmaceutical filling and packaging operations. Develop URS, DS, and FS; collaborate with vendors and cross-functional teams; support FAT, SAT, commissioning, and qualification activities; conduct reliability and optimization studies; and lead engineers and project stakeholders in a cGMP environment.

Lead design, commissioning, qualification, validation, troubleshooting, and optimization of filling and packaging systems in sterile pharmaceutical manufacturing environments. Develop URS, DS, and FS documents; coordinate vendors and cross-functional teams; support FAT, SAT, commissioning, and qualification activities; and lead engineers and project stakeholders. The role requires pharmaceutical or biotech experience, cGMP knowledge, leadership, occasional travel or extended hours, and work at client facilities in Portland, Oregon.

Leads MMR Consulting’s India business with full P&L ownership, business development, CQV technical oversight, regulatory quality accountability, and team growth. The role manages budgets, pricing, proposals, pharmaceutical and biotechnology client relationships, validation strategy, GMP and data integrity standards, hiring, training, performance management, and succession planning. The leader will expand India delivery capabilities for local and global projects while serving as the senior technical authority for commissioning, qualification, and validation work.

Leads MMR Consulting’s India business with full P&L accountability, business development, CQV technical oversight, regulatory quality ownership, and team growth. The role requires managing budgets, pricing, proposals, client relationships, validation strategies, GMP and data integrity standards, hiring, training, performance management, and succession planning. The leader will expand pharmaceutical and biotechnology consulting delivery across India and global projects while serving as the senior technical authority for commissioning, qualification, and validation work.

Provides owner-representative mechanical engineering, field engineering, quality control, installation oversight, testing, and commissioning support for wastewater treatment capital projects. Reviews mechanical and piping designs, verifies equipment and materials, coordinates contractors, inspects installations, witnesses testing, tracks RFIs and submittals, supports turnover documentation, and reports project progress. Requires mandatory WWTP experience and leadership of junior engineers.

Provides field engineering, quality control, installation verification, testing, commissioning, and documentation support for industrial electrical systems ranging from 12.4 kV to 120 V. Coordinates with construction managers, contractors, and client stakeholders; reviews designs, verifies equipment and materials, conducts inspections, tracks RFIs and submittals, supports turnover documentation, and reports project progress.

Supports commissioning, qualification, validation, and startup of pharmaceutical and biopharmaceutical equipment, utilities, facilities, and process systems. Develops and executes DQ, FAT, SAT, IQ, OQ, and PQ deliverables; supports validation plans, risk-based qualification, regulatory compliance, and project coordination. The role includes field execution, contractor supervision, client-site work, occasional travel, construction-site visits, and potential extended-hours support during project phases.

Perform commissioning, qualification, validation, and start-up activities for pharmaceutical and biopharmaceutical equipment, utilities, facilities, and process systems. Develop and execute qualification deliverables including DQ, FAT, SAT, IQ, OQ, and PQ; support validation plans, risk-based approaches, field testing, regulatory compliance, and project coordination. The role involves client-site work, contractor supervision, occasional travel, shutdown support, and collaboration across engineering and operational teams.

Leads commissioning, qualification, validation, and startup activities for biopharmaceutical manufacturing systems, facilities, utilities, and process equipment. Manages qualification deliverables, risk assessments, protocols, testing, deviations, and final reports. Provides technical leadership to engineers, coordinates cross-functional project teams, manages client relationships, schedules, budgets, and supports business development. Requires extensive pharmaceutical or biotechnology experience, including upstream or downstream bioprocess C&Q.

Support commissioning, qualification, validation, and start-up of pharmaceutical and biopharmaceutical process equipment, utilities, facilities, and automation systems. Develop and execute qualification deliverables, validation plans, protocols, and risk assessments while coordinating cross-functional teams, contractors, vendors, and clients. Work primarily at client sites in the Denver/Boulder area, with occasional travel, construction-site visits, shutdown support, and extended hours. Responsibilities may also include project coordination, scheduling, budgeting, client management, and technical support for business development.

Supports commissioning, qualification, validation, and start-up of pharmaceutical and biopharmaceutical systems, equipment, utilities, and facilities. Develops and executes qualification protocols, validation plans, risk assessments, and testing deliverables under cGMP requirements. Coordinates cross-functional teams, contractors, vendors, and client stakeholders while supporting project delivery, site activities, and occasional FAT travel. The role may also involve supervising engineers, scheduling, budgeting, client management, and extended-hours support during project phases.

Lead commissioning, qualification, validation, and startup activities for biopharmaceutical process equipment, facilities, and utilities. Develop and execute risk assessments, DQ, FAT, SAT, IQ, OQ, PQ, protocols, reports, and deviation resolution. Guide engineering teams, coordinate cross-functional stakeholders, manage client relationships, schedules, and budgets, and support business development. The role requires extensive pharmaceutical or biotech C&Q experience, occasional travel, site visits, and possible shutdown or extended-hours support.