CQV Automation Engineer – Life Sciences

Verista, Inc.; Columbus (OH); On-site; USD 74,000 - 118,000; Full time

Benefits offered by this job

Competitive pay and incentives

Health Savings Account

Paid Time Off and Holidays

Disability Insurance

Job summary

Verista, Inc. seeks an Equipment Engineer to support the design, installation, and qualification of automated manufacturing and packaging equipment in GMP environments.

You will troubleshoot mechanical and electrical systems, collaborate with vendors and cross-functional teams, and contribute to commissioning activities on 2nd/3rd shifts. The ideal candidate has 2–5 years of experience in CQV, commissioning, automation, or validation, and a hands-on engineering approach.

Qualifications

• 2–5 years of experience in equipment engineering, manufacturing engineering, CQV, commissioning, automation, or validation.
• Experience troubleshooting automated manufacturing or packaging equipment.
• Strong understanding of mechanical and electrical systems, automation, and industrial controls.
• Experience with GMP-regulated pharmaceutical, biotech, medical device, or similar manufacturing environments.
• Hands-on engineering approach and ability to work with cross-functional teams.

Responsibilities

• Support equipment integration, optimization, and production ramp-up activities.
• Review equipment designs, specifications, drawings, manuals, and control documentation.
• Partner with vendors and internal engineering teams to identify root causes and implement equipment improvements.
• Provide hands-on engineering support during 2nd/3rd shift commissioning and production activities.
• Document technical issues, test results, deviations, and corrective actions in a GMP environment.

Skills

Equipment engineering

Manufacturing engineering

CQV

Commissioning

Automation

Validation

Tools

ATS

IMA

Dividella

Job description

Verista, Inc. seeks an Equipment Engineer to support the design, installation, and qualification of automated manufacturing and packaging equipment in GMP environments.

You will troubleshoot mechanical and electrical systems, collaborate with vendors and cross-functional teams, and contribute to commissioning activities on 2nd/3rd shifts. The ideal candidate has 2–5 years of experience in CQV, commissioning, automation, or validation, and a hands-on engineering approach.