Job Description

About Us

At cGMP Consulting, we specialize in providing expert validation, qualification, and compliance services to the life sciences industry. Our team works with clients to ensure their facilities, equipment, and processes meet regulatory standards, enabling the safe and efficient production of pharmaceuticals.
cGMP Consulting is based in Lake Forest, IL. Our main client locations are Melrose Park, IL, North Chicago, IL, Waukegan, IL and Pleasant Prairie, WI. 

Position Summary

cGMP Consulting is seeking an entry level engineer to support a short-term initiative to digitally capture and document format parts used in pharmaceutical production equipment. This role involves operating 3D scanning equipment and associated software to generate accurate digital models of mechanical components critical to manufacturing processes. The engineer will ensure scanned data meets dimensional accuracy and documentation standards, enabling effective archiving, reverse engineering, or equipment modification. This position requires close collaboration with engineering, maintenance, and quality teams to ensure scanned outputs align with GMP expectations and equipment specifications. The assignment is expected to last approximately three months.

This role is full time for a limited duration with potential for extension or addition projects after completion.

Responsibilities 

• Operate 3D scanning equipment to capture accurate digital models of format parts used in pharmaceutical production equipment.
• Prepare, clean, and position parts for scanning to ensure high-quality data capture.
• Process and refine scanned data using specialized software to generate usable digital files and models.
• Verify dimensional accuracy of scanned outputs against specifications and drawings.
• Document scanning activities and maintain records in compliance with GMP and internal quality standards.
• Collaborate with engineering and maintenance teams to confirm part details and resolve discrepancies.
• Support integration of scanned files into design, reverse engineering, or equipment modification projects.
• Ensure proper handling and storage of format parts during scanning activities to prevent damage or contamination.
• Assist in preparing scanned data and documentation for audit readiness and inspection support.
• Contribute to continuous improvement by identifying opportunities to streamline scanning workflows and enhance data quality.

Requirements 

• Bachelors’ degree in Engineering, Science, or a related field of study. 
• 0-2 years’ experience in a GMP manufacturing environment. 
• Experience with 3D scanning technologies such as laser scanners, structured light scanners, or CT scanning systems.
• Familiar with regulatory (FDA) requirements. 
• Business minor or coursework is strongly encouraged. 
• Advanced critical thinking and technical writing skills.
• Strong organizational, communication, and interpersonal skills. 

Compensation and Benefits 

• Expected pay range per year: $55,000-$75,000 USD 
• Expected benefits include: Medical, Dental, Vision, PTO, 401K 

Disclaimer 

The duties and responsibilities described are not a comprehensive list and additional tasks may be assigned to the employee from time to time; or the scope of the job may change as necessitated by business demands. All duties and responsibilities are subject to possible modification to reasonably accommodate individuals with disabilities. The requirements listed are the minimum levels of knowledge, skills, or abilities necessary to perform this job successfully. The company is an Equal Opportunity Employer, drug-free workplace, and complies with ADA regulations as applicable. 

Job Tags

Full time, Temporary work,

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