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.
- Experiencewith 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: $55000-$75000 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.
Required Experience:
Junior IC
About UsAt 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 pharmace...
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.
- Experiencewith 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: $55000-$75000 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.
Required Experience:
Junior IC
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