Project Engineer - GMP

LVI Associates; Columbus (OH); Vor Ort; USD 74.000 - 120.000; Vollzeit

Benefits dieser Stelle

401(k) plan

Healthcare

PTO

Tuition reimbursement

Zusammenfassung

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.

Qualifikationen

• 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.

Aufgaben

• 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.

Kenntnisse

CQV experience

Troubleshooting automation

Mechanical systems

Electrical systems

GMP pharma experience

Analytical skills

Cross-functional collaboration

Documentation skills

Ausbildung

Engineering degree

Jobbeschreibung

Project Engineer

Location: Columbus, OH
Salary: $74,000 - $120,000

Overview

Support equipment commissioning, qualification, startup, and production activities within a GMP-regulated pharmaceutical manufacturing environment. This hands-on role focuses on troubleshooting, validation, and equipment optimization across automated manufacturing systems.

Key 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

Requirements

• 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 systems, electrical systems, and industrial automation


• 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

Qualifications

• Engineering degree or related technical background preferred


• Hands-on approach to troubleshooting and process improvement


• Strong communication and documentation skills


• Ability to manage multiple priorities independently


• Experience supporting validation and qualification activities

Why Join?

• Support cutting-edge pharmaceutical and biotech manufacturing projects


• Gain exposure to CQV, commissioning, validation, and automation engineering


• Strong career growth opportunities in a high-growth organization


• Competitive compensation and bonus potential


• Comprehensive benefits package including 401(k), healthcare, PTO, and tuition reimbursement


• Collaborative and team-oriented environment focused on development and success