Manufacturing Engineer II

We are partnering with our client, a leading organization in the medical device industry, to identify a Manufacturing Engineer II for a long-term contract opportunity.

This is an excellent opportunity to contribute to process improvement, manufacturing excellence, and regulatory-compliant product production within a highly regulated environment.

In this role, you will help optimize manufacturing processes, support continuous improvement initiatives, and ensure manufacturing operations meet quality, compliance, and production objectives. Your work will directly impact efficiency, product quality, and operational performance.

Location & Schedule

• Location: Naperville, IL
• Schedule: 5 days/week onsite
• Contract Position
• Long-term engagement (1+ year anticipated)

The Manufacturing Engineer II will apply engineering principles, problem-solving skills, and process improvement methodologies to support and optimize manufacturing operations.

This role will work closely with production teams, quality, compliance, technicians, and project stakeholders to drive process enhancements, execute validation activities, and resolve manufacturing-related issues.

Key Responsibilities

• Optimize manufacturing processes using Lean, Six Sigma, and continuous improvement methodologies.
• Design, improve, and support manufacturing equipment, tooling, fixtures, and related processes.
• Develop and execute validation protocols, studies, and process qualification activities.
• Analyze manufacturing data and present findings, recommendations, and technical reports.
• Investigate and resolve manufacturing and compliance issues, including CAPAs, non-conformances, and audit observations.
• Create work instructions, technical documentation, and training materials for production teams.
• Develop project plans, risk assessments, and timelines to ensure successful project delivery.
• Provide technical guidance and direction to manufacturing technicians.
• Coordinate testing activities and manufacturing support efforts.
• Collaborate with cross-functional teams to improve operational efficiency, quality, and compliance outcomes.

Required Qualifications

• Bachelor's degree in Engineering.
• 2-4 years of engineering experience in a manufacturing environment.
• Experience supporting manufacturing process improvement initiatives.
• Understanding of Lean Manufacturing and/or Six Sigma methodologies.
• Experience developing and executing process validations, testing, or qualification activities.
• Knowledge of FDA regulations and quality systems within a regulated industry.
• Strong analytical, troubleshooting, and problem-solving skills.
• Experience working with manufacturing, laboratory, or industrial equipment.
• Proficiency with Microsoft Office Suite; MS Project experience preferred.
• Strong communication, documentation, and stakeholder management skills.
• Ability to manage multiple priorities in a fast-paced environment.
• Strong attention to detail and commitment to quality.

Nice-to-Have Qualifications

• Medical device industry experience.
• CAD experience.
• Experience working in cleanroom manufacturing environments.
• Exposure to CAPA investigations and regulatory audits.
• Experience training technicians or supporting manufacturing teams.
• Statistical analysis experience for manufacturing processes.

What Makes This Role Unique

• Opportunity to support a globally recognized medical device manufacturing environment.
• Direct involvement in process optimization and continuous improvement initiatives.
• Long-term contract engagement with potential extension opportunities.
• Exposure to cross-functional engineering, quality, and manufacturing teams.
• Multiple openings available with an immediate hiring need.

Interview Process

• Initial 30-minute virtual interview with Hiring Manager
• Team interview (onsite or virtual)
• Interviews commencing immediately
• Candidate must provide a screenshot confirming attendance at the virtual interview

Beacon Hill is an Equal Opportunity Employer that values the strength diversity brings to the workplace. Individuals with Disabilities and Protected Veterans are encouraged to apply.

Completion of this form is voluntary and will not affect your opportunity for employment, or the terms or conditions of your employment. This form will be used for reporting purposes only and will be kept separate from all other records.

California residents: Qualified applications with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.

If you're a Manufacturing Engineer looking to make an impact in a regulated manufacturing environment, we'd love to connect with you.

Client details will remain confidential throughout the hiring process and will be shared with qualified candidates at the appropriate stage.