via The BIG Jobsite
$40K - 70K a year
Assist in project documentation, asset management, and compliance activities within a GMP-regulated environment.
Requires a Bachelor's in Engineering, 1-3 years of experience, and familiarity with equipment, utility systems, and GMP standards.
Qualifications: • Bachelor’s degree in Engineering (Mechanical, Electrical, Chemical, or related field preferred) • 1–3 years of experience in an engineering or technical support role, preferably in a pharmaceutical or regulated industry • Understanding of equipment and utility systems in a manufacturing or plant setting • Strong organizational and communication skills • Proficiency in Microsoft Office Suite (Word, Excel, Project) Pluses • Familiarity with validation documentation and GMP principles is a plus Job description We are seeking a detail-oriented and proactive Project Engineer to assist our pharmaceutical client’s engineering team. This contract role is ideal for an engineer with a foundational understanding of equipment and utility systems in a GMP-regulated environment. The position will primarily support documentation and administrative tasks related to project execution, asset management, and compliance. You will work closely with Plant/Utility and Project Engineers to ensure timely and accurate completion of project documentation, approvals, and coordination activities. Familiarity with validation processes and pharmaceutical manufacturing standards is a plus. Key Responsibilities: • Draft and route Project Scope Documents for review and approval • Support equipment and asset enrollment into GMP systems • Assist in creating and maintaining project schedules and timelines • Coordinate decommissioning of legacy assets in compliance with site procedures • Contribute to cost estimation for new capital projects • Manage documentation workflows including form completion, routing, and approval tracking • Collaborate with engineering teams to ensure technical accuracy and regulatory alignment • Provide general project management support across multiple initiatives • Maintain organized records in accordance with GMP documentation standards
This job posting was last updated on 1/12/2026