Pharma Site Integration Lead for Brownfield Projects

Process Automation – Controls.Instruments.Validations, Inc.; San Juan (PR); On-site; USD 120,000 - 180,000; Full time

Job summary

PACIV is seeking a Site Integration Project Manager to lead planning and execution of site integration and utility tie-in projects in a GMP environment. You will coordinate scopes, budgets, and schedules while ensuring minimal disruption to ongoing pharmaceutical production.

Ideal candidates have 12+ years in capital projects, including brownfield or utility tie-in work in pharma, biotech, or chemical facilities, with strong change control and MOC experience.

Qualifications

• Bachelor's degree in Mechanical, Chemical, Civil Engineering, Construction Management, or a related field.

Responsibilities

• Manage a portfolio of site integration and utility tie-in projects from planning through turnover.
• Coordinate project scope, budget, schedule, contractor performance, and project risks.
• Partner with Operations to plan shutdowns, production impacts, and change control activities.
• Coordinate utility tie-ins and modifications with engineering, construction, and operations teams.
• Lead contractor activities in operating facilities, including site access, training, GMP requirements, and restricted area compliance.
• Promote safe execution and ensure compliance with GMP, HSE, and Management of Change (MOC) requirements.
• Monitor project progress, costs, schedules, and risks, providing regular updates to project stakeholders.
• Ensure successful project completion with minimal disruption to plant operations.

Skills

Leadership

Stakeholder management

Cross-functional coordination

GMP compliance

Project controls

Planning

Problem-solving

Communication

Education

Bachelor's degree in Mechanical, Chemical, Civil Engineering or Construction Management

Job description

PACIV is seeking a Site Integration Project Manager to lead planning and execution of site integration and utility tie-in projects in a GMP environment. You will coordinate scopes, budgets, and schedules while ensuring minimal disruption to ongoing pharmaceutical production.

Ideal candidates have 12+ years in capital projects, including brownfield or utility tie-in work in pharma, biotech, or chemical facilities, with strong change control and MOC experience.