6565 - Project Engineer

DescriptionVerista’s 500 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world’s most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities.

Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day.

Company Culture Guidelines & Values:

• We empower and support our colleagues

• We commit to client success at every turn

• We have the courage to do the right thing

• We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged.

• We constantly acquire new skills and learn from our experiences to enhance our collective expertise

Project Engineer Responsibilities:

• Support equipment installation, commissioning, startup, and qualification activities.

• Troubleshoot mechanical, electrical, controls, instrumentation, sensors, servos, pneumatics, and automation issues.

• Execute equipment functional testing and CQV protocols, including IQ/OQ and performance testing.

• Review equipment designs, specifications, drawings, manuals, and control documentation.

• Partner with vendors and internal engineering teams to identify root causes and implement equipment improvements.

• Support equipment integration, optimization, and production ramp-up activities.

• Document technical issues, test results, deviations, and corrective actions in a GMP environment.

• Provide hands-on engineering support during 2nd/3rd shift commissioning and production activities.

Requirements:

• 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.

• Strong analytical and problem-solving skills with a hands-on engineering approach.