GMP Project Engineer: CQV, Commissioning & Automation

LVI Associates; Columbus (OH); On-site; USD 74,000 - 120,000; Full time

Benefits offered by this job

401(k) plan

Healthcare

PTO

Tuition reimbursement

Job summary

LVI Associates in Columbus, OH is seeking a hands-on Project Engineer to support commissioning, qualification, startup, and production activities within a GMP-regulated pharmaceutical manufacturing environment.

The role focuses on troubleshooting, validation, and optimization across automated manufacturing systems, with responsibilities spanning IQ/OQ execution, equipment documentation, and cross-functional collaboration to resolve issues and ensure smooth project ramp-up.

Qualifications

• 2–5 years of experience in project engineering, CQV, validation, commissioning, manufacturing engineering, or automation.
• Experience troubleshooting automated manufacturing or packaging equipment.
• Understanding of mechanical, electrical, and industrial automation systems.
• Experience in GMP-regulated pharmaceutical, biotech, or medical device environments.
• Strong analytical and problem-solving skills.
• Ability to collaborate with cross-functional teams and vendors.

Responsibilities

• Support equipment installation, startup, and qualification activities.
• Execute IQ/OQ protocols and performance testing.
• Troubleshoot mechanical, electrical, controls, and automation issues.
• Review equipment documentation and technical specifications.
• Partner with vendors and internal teams to resolve equipment issues.
• Support equipment integration and production ramp-up.
• Document deviations, investigations, and corrective actions.
• Provide hands-on support during commissioning and production activities.

Skills

CQV experience

Troubleshooting automation

Mechanical systems

Electrical systems

GMP pharma experience

Analytical skills

Cross-functional collaboration

Documentation skills

Education

Engineering degree

Job description

LVI Associates in Columbus, OH is seeking a hands-on Project Engineer to support commissioning, qualification, startup, and production activities within a GMP-regulated pharmaceutical manufacturing environment.

The role focuses on troubleshooting, validation, and optimization across automated manufacturing systems, with responsibilities spanning IQ/OQ execution, equipment documentation, and cross-functional collaboration to resolve issues and ensure smooth project ramp-up.