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Cqv Project Engineers

  • Cqv Project Engineers job type Posted on: Oct 14, 2026
  • Cqv Project Engineers experience level Stellent IT LLC
  • Cqv Project Engineers employment type Columbus, Ohio
  • Cqv Project Engineers employment type Onsite
  • Cqv Project Engineers salary Full-time

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Job Title :

Cqv Project Engineers

Job Type :

Full-Time

Job Location :

Columbus Ohio United States

Remote :

No

Jobcon Logo Job Description :

TITLE - CQV Project Engineers -

Columbus ,OH

Lead equipment commissioning, startup, qualification, and performance activities.

Provide hands-on engineering support for complex mechanical, electrical, controls, instrumentation, servo, vision, and automation issues.
Lead troubleshooting, root-cause analysis, and implementation of corrective and equipment improvement actions.
Review and approve equipment designs, specifications, drawings, control strategies, and technical documentation.
Lead equipment integration, optimization, and production ramp-up activities.
Serve as the technical interface with equipment OEMs and vendors, driving issue resolution and equipment performance.
Develop and execute engineering and CQV test strategies, including FAT/SAT, IQ/OQ, and performance testing.
Identify opportunities to improve equipment reliability, throughput, cycle time, quality, and maintainability.
Provide technical direction and mentorship to junior engineers and CQV personnel.
Support deviations, change controls, CAPAs, and technical investigations within a GMP environment.
Provide engineering leadership during off-shift commissioning, qualification, and production support.

Qualifications
5+ years of experience in equipment engineering, CQV, commissioning, automation, manufacturing engineering, or a related discipline.
Strong hands-on experience with automated manufacturing and packaging equipment.
Demonstrated expertise troubleshooting mechanical, electrical, controls, and automation systems.
Experience with PLC/HMI systems, servos, sensors, vision systems, robotics, and automated equipment preferred.
Experience in a GMP-regulated pharmaceutical, biotech, medical device, or similar manufacturing environment.
Strong understanding of equipment qualification, commissioning, and validation principles.
Proven ability to lead technical issues, vendors, projects, and cross-functional engineering teams.
Excellent analytical, troubleshooting, communication, and technical documentation skills.
Experience with ATS, IMA, Dividella, or similar equipment is highly preferred.
Willingness to work 2nd and/or 3rd shift as required.

Jobcon Logo Position Details

Posted:

Oct 14, 2026

Reference Number:

52054-6911

Employment:

Full-time

City:

Columbus

Job Origin:

CIEPAL_ORGANIC_FEED

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TITLE - CQV Project Engineers -

Columbus ,OH

Lead equipment commissioning, startup, qualification, and performance activities.

Provide hands-on engineering support for complex mechanical, electrical, controls, instrumentation, servo, vision, and automation issues.
Lead troubleshooting, root-cause analysis, and implementation of corrective and equipment improvement actions.
Review and approve equipment designs, specifications, drawings, control strategies, and technical documentation.
Lead equipment integration, optimization, and production ramp-up activities.
Serve as the technical interface with equipment OEMs and vendors, driving issue resolution and equipment performance.
Develop and execute engineering and CQV test strategies, including FAT/SAT, IQ/OQ, and performance testing.
Identify opportunities to improve equipment reliability, throughput, cycle time, quality, and maintainability.
Provide technical direction and mentorship to junior engineers and CQV personnel.
Support deviations, change controls, CAPAs, and technical investigations within a GMP environment.
Provide engineering leadership during off-shift commissioning, qualification, and production support.

Qualifications
5+ years of experience in equipment engineering, CQV, commissioning, automation, manufacturing engineering, or a related discipline.
Strong hands-on experience with automated manufacturing and packaging equipment.
Demonstrated expertise troubleshooting mechanical, electrical, controls, and automation systems.
Experience with PLC/HMI systems, servos, sensors, vision systems, robotics, and automated equipment preferred.
Experience in a GMP-regulated pharmaceutical, biotech, medical device, or similar manufacturing environment.
Strong understanding of equipment qualification, commissioning, and validation principles.
Proven ability to lead technical issues, vendors, projects, and cross-functional engineering teams.
Excellent analytical, troubleshooting, communication, and technical documentation skills.
Experience with ATS, IMA, Dividella, or similar equipment is highly preferred.
Willingness to work 2nd and/or 3rd shift as required.

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