ATL01-042525 Principal Manufacturing Engineer-Illinois

Validation & Engineering Group, Inc.; Kankakee (IL); On-site; USD 80,000 - 110,000; Full time

Job summary

An established industry player is seeking a Principal Manufacturing Engineer to enhance operations in Kankakee, Illinois. This pivotal role involves providing hands-on technical support for manufacturing processes, troubleshooting complex equipment issues, and driving process improvements. The successful candidate will collaborate with cross-functional teams, mentor junior members, and ensure compliance with GMP standards. If you are passionate about engineering and eager to make a significant impact in a dynamic environment, this opportunity is perfect for you.

Qualifications

• 5+ years in pharmaceutical or biotech manufacturing required.
• Experience in regulated environments like cGMP preferred.

Responsibilities

• Provide technical support for manufacturing operations and troubleshoot equipment issues.
• Lead investigations of production incidents and manage quality records.

Skills

Engineering Principles

Troubleshooting

Problem-Solving

GMP Documentation

Mechanical Aptitude

Collaboration

Education

Bachelor’s in Engineering

Life Sciences Degree

Tools

SAP

GLIMS

Job description

ATL01-042525 Principal Manufacturing Engineer-Illinois

ATL01-042525 Principal Manufacturing Engineer-Illinois

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About Validation & Engineering Group (V&EG)

Validation & Engineering Group (V&EG) is a leading provider of commissioning, qualification, validation, engineering, and compliance services to the pharmaceutical, biotech, medical device, and chemical industries. With a team of dedicated professionals across the United States, we partner with our clients to deliver innovative solutions and exceptional service. We are currently seeking a Principal Manufacturing Engineer to support our client in Kankakee, Illinois.

Job Summary

The Principal Manufacturing Engineer will be a key member of the Manufacturing Support Team, providing hands-on technical support to Bulk or Fill/Finish Operations. This role serves the night shift as the first line of response for process and equipment-related issues, driving resolution efforts and ensuring production continuity. The successful candidate will support investigations, process improvements, and documentation while mentoring junior team members and collaborating across departments to optimize operations.

Key Responsibilities

• Serve as front-line technical support for manufacturing operations, troubleshooting complex equipment and automation issues.
• Lead investigations and resolution of production incidents, including major automation interventions as needed.
• Author, revise, and approve GMP documentation (batch records, procedures, work instructions, training materials).
• Own and manage quality records (deviations, incidents, CAPAs, and change controls).
• Drive and implement process improvement initiatives in collaboration with cross-functional teams.
• Support internal audits and external inspections; provide support for project implementation.
• Serve as a technical point of contact for process development projects and cross-functional troubleshooting.
• Provide mentoring and coaching to junior support team members.
• Support training of manufacturing staff on new processes and systems (SAP, GLIMS, etc.).
  
  

Required Skills & Competencies

• Strong understanding of engineering principles, equipment functionality, and automation systems.
• High mechanical aptitude and hands-on troubleshooting experience.
• Strong problem-solving skills with attention to detail.
• Familiarity with regulated manufacturing environments (e.g., cGMP, OSHA, EPA).
• Experience working in cleanroom environments is preferred.
• Ability to work independently and collaboratively in a fast-paced, 24x7 operation.
  
  

Minimum Education Requirements

• Bachelor’s degree in Engineering, Life Sciences, or related field preferred.
• Equivalent experience in pharmaceutical manufacturing will be considered.
  
  

Minimum Experience Requirements

• 5+ years of experience in pharmaceutical or biotech manufacturing required.
• Prior experience supporting vaccine, fill/finish, or bulk manufacturing operations strongly preferred.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Contract

Job function

• Job function

  Strategy/Planning and Information Technology

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