Senior Project Engineer – GMP Facilities & Validation

Syner-G; Marlborough (MA); On-site; USD 90,000 - 120,000; Full time

Job summary

Syner-G in Marlborough, MA, seeks an engineer to support capital projects from design through commissioning, qualification, and startup activities within a GMP-regulated environment.

You will coordinate cross-functional teams, develop and execute commissioning protocols, and ensure compliance with safety, quality, and regulatory requirements, while traveling to client sites up to 100% based on project needs.

Qualifications

• Bachelor's degree in Engineering or related technical field.
• 2–5 years of GMP-regulated pharma/biotech/facility experience.
• Experience supporting capital projects and validation activities.
• Hands-on startup, commissioning, qualification, or validation experience.

Responsibilities

• Support capital projects from design through commissioning, qualification, validation and startup.
• Perform startup and commissioning of building and utility systems (HVAC, water, electrical, fire protection).
• Support validation/qualification activities and develop reports and protocols.
• Generate and manage engineering/validation documentation and walkdowns.
• Coordinate with cross-functional teams to meet milestones and ensure GMP compliance.

Skills

Project mgmt

Documentation

Communication

Regulatory compliance

Education

Bachelor's Degree in Engineering

Tools

KNEAT

BMS/PCS/CMMS

Job description

Syner-G in Marlborough, MA, seeks an engineer to support capital projects from design through commissioning, qualification, and startup activities within a GMP-regulated environment.

You will coordinate cross-functional teams, develop and execute commissioning protocols, and ensure compliance with safety, quality, and regulatory requirements, while traveling to client sites up to 100% based on project needs.