Pharma Project Engineer: CQV, Automation & Validation

Katalyst CRO; Illinois; On-site; USD 90,000 - 130,000; Full time

Job summary

Katalyst CRO is seeking a Project Engineer in Illinois to manage medium-size capital projects from concept through closure in a GMP/pharma environment. You will work with Operations, Maintenance, Engineering, and suppliers to deliver equipment and facility projects on schedule and within budget.

The role requires a Bachelor's degree in engineering, strong PLC/control systems knowledge, and experience with validation activities such as FAT/SAT.

Qualifications

• Proven ability to manage medium-size projects from concept through closure.
• Strong technical background in pharmaceutical/medical device projects.
• Experience with validation activities and equipment commissioning.

Responsibilities

• Support capital projects in the manufacturing plant, including front end planning.
• Coordinate multiple parties to complete project scopes on schedule and within budget.
• Assist with design of new equipment systems, budgeting, scheduling, and construction management.
• Develop project schedules and track progress to meet milestones and deadlines.
• Review drawings, supervise contractors, and participate in final project acceptance.

Skills

Project management

Engineering knowledge

Financial management

Contractor management

Pharma GMP familiarity

Leadership

Communication

PLC controls

Education

Bachelor's Degree in Engineering

Job description

Katalyst CRO is seeking a Project Engineer in Illinois to manage medium-size capital projects from concept through closure in a GMP/pharma environment. You will work with Operations, Maintenance, Engineering, and suppliers to deliver equipment and facility projects on schedule and within budget.

The role requires a Bachelor's degree in engineering, strong PLC/control systems knowledge, and experience with validation activities such as FAT/SAT.