Manufacturing Engineer II

Title: Manufacturing Engineer II

Pay: $40.00 - $45.00/hr

Location: Naperville, IL

Schedule: Standard Office Hours

Duration: 12-Month Contract




Support the optimization and continuous improvement of manufacturing processes by applying engineering principles, technical expertise, and structured problem-solving methodologies. This role focuses on process development, validation, compliance, and cross-functional collaboration to improve manufacturing efficiency, quality, and operational performance.

Responsibilities

• Optimize manufacturing processes using continuous improvement methodologies such as Lean and Six Sigma.
• Design or redesign manufacturing equipment, tools, fixtures, and processes to improve efficiency and product quality.
• Develop, execute, and document process validation and qualification protocols, including analysis of test results and recommendations for improvement.
• Investigate and resolve manufacturing and quality issues, including CAPAs, non-conformances, and audit findings.
• Create and maintain manufacturing documentation, including work instructions, procedures, and training materials.
• Develop project plans, perform risk assessments, and manage project deliverables to meet business objectives.
• Provide technical support to manufacturing operations and oversee day-to-day engineering activities.
• Train and mentor manufacturing technicians, provide technical guidance, and coordinate testing activities.
• Collaborate with cross-functional teams to support manufacturing initiatives and process improvements.
• Perform additional engineering duties as assigned.

Qualifications

Required

• Bachelor's degree in Engineering or a related technical discipline.
• 2–4 years of manufacturing engineering experience.
• Working knowledge of manufacturing process optimization and engineering principles.
• Experience with process validation, qualification protocols, and technical documentation.
• Understanding of statistical analysis and problem-solving methodologies.
• Familiarity with FDA-regulated manufacturing environments and quality systems.
• Knowledge of manufacturing equipment and industrial or laboratory environments.
• Proficiency with Microsoft Office applications; experience with Microsoft Project preferred.
• Strong analytical, organizational, communication, and documentation skills.
• Ability to manage multiple priorities in a fast-paced, team-oriented environment.
• Strong interpersonal skills with the ability to collaborate across departments and with external partners.
• Commitment to maintaining quality, environmental health and safety, and regulatory compliance.

Preferred

• Experience with Lean Manufacturing and Six Sigma methodologies.
• CAD experience.
• Experience supporting cleanroom or regulated manufacturing operations

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