Lead Process Engineer

The Lead Process Engineer position is an exciting opportunity to join PM Group’s quickly growing Outsourced Technical Services(OTS) team for a client in the Greater Boston area .

Outsourced Technical Services (OTS) is an integral part of PM Group’s ability to support clients across the complete project life cycle.

We have over 50 years’ industry experience, strong technical knowledge and integrated resources.

Clients look to us to provide experienced technical professionals that complement their project teams.

Together we are sharing knowledge, learning, growing and continuing to be an integral part of supporting PM Group’s ongoing expansion in the US.

We are seeking an experienced Lead Process Engineer to provide technical and project leadership for the deployment of process equipment within a GMP-regulated biopharmaceutical manufacturing environment.

This role will oversee equipment delivery, installation, integration, commissioning, qualification, and operational handover while ensuring compliance with quality, safety, and regulatory requirements.

PM Group is an employee owned, international project delivery firm with a team of 4,000+ people.

We are world leaders in the pharma, food, biotech, medical technology and mission critical sectors.

From our network of offices in Europe, Asia and the US, we work with the world's leading organizations.

We are focused on growing a sustainable business centered on our people, our clients and trade partners.

• Lead process equipment implementation projects from planning through operational handover.
• Manage project schedules, change controls, risk assessments, and cross-functional coordination activities.
• Oversee equipment delivery, installation, commissioning, startup activities, and punch-list resolution.
• Support asset onboarding, calibration programs, preventive maintenance planning, and spare parts management.
• Coordinate integration activities with automation, process control systems, digital systems, and computerized system validation (CSV) teams.
• Lead qualification activities, discrepancy investigations, and lifecycle documentation development.
• Ensure operational readiness through training coordination, EHS reviews, GMP release activities, and successful turnover to operations.
• Collaborate with Manufacturing, Engineering, Quality, Validation, Facilities, and Project Management teams to deliver project objectives.