Pharma Clean Utilities Engineer - Commissioning Lead

MMR Consulting; Philadelphia (Philadelphia County); On-site; USD 120,000 - 150,000; Full time

Job summary

MMR Consulting is actively seeking a seasoned commissioning, qualification and validation engineer to join our growing team of engineers in the United States. You will work on projects involving design, start-up, and qualification of pharmaceutical facilities and utilities.

You will develop PFDs, P&IDs, IQ/OQ/PQ, and FAT plans, while guiding cross-functional teams and ensuring compliance with cGMP standards. Occasional travel and client-site work are expected.

Qualifications

• 5+ years of commissioning, qualification or validation of clean utility systems.
• Experience in pharmaceutical/biotech with cGMP knowledge.
• Experience with PW/WFI/CS and HVAC systems.
• Ability to lead cross-functional teams and manage multiple projects.
• Travel may be required.

Responsibilities

• Guide design, commissioning, qualification and start-up of pharmaceutical facilities and utilities.
• Develop deliverables such as PFDs, P&IDs, specifications, IQ/OQ/PQ and FAT plans.
• Support field installation and testing of validation protocols.
• Serve as technical SME on clean utilities and regulatory requirements.
• Lead project lifecycle activities to meet quality and engineering specs.
• Coordinate cross-functional project reviews and progress updates.
• Travel to client sites or vendors as needed.
• Support business development and client relationship management.

Skills

Commissioning/Qualification

Project Management

Leadership

Mentorship

cGMP Knowledge

Engineering Leadership

Education

Engineering degree (Mechanical/Electrical/Chemical)

Job description

MMR Consulting is actively seeking a seasoned commissioning, qualification and validation engineer to join our growing team of engineers in the United States. You will work on projects involving design, start-up, and qualification of pharmaceutical facilities and utilities.

You will develop PFDs, P&IDs, IQ/OQ/PQ, and FAT plans, while guiding cross-functional teams and ensuring compliance with cGMP standards. Occasional travel and client-site work are expected.