Pharma GMP Project Engineer – CQV & Automation

Katalyst CRO; Illinois; On-site; USD 85,000 - 110,000; Full time

Job summary

Katalyst CRO is seeking a Project Engineer in Illinois who will oversee medium size projects in the pharmaceutical sector. Responsibilities include capital project support, coordinating project scopes, managing equipment design, and ensuring compliance with GMP standards. The ideal candidate will have a Bachelor's Degree in Engineering, strong communication skills, and over four years of experience in a related field. This role requires technical knowledge of pharmaceutical equipment and project management expertise.

Qualifications

• 4+ years of experience in project engineering, preferably in a GMP-regulated environment.
• Technical background in pharmaceutical industry.
• Expertise in equipment design and specifications.
• Strong collaboration skills with diverse groups.

Responsibilities

• Support capital projects in the manufacturing plant.
• Coordinate project scopes on schedule and within budget.
• Assist in design and management of new equipment systems.
• Develop and track project schedules and documentation.

Skills

Communication Skills

Project Management

Engineering Knowledge

Pharmaceutical/Medical Device Knowledge

Interpersonal Skills

Automation & Controls Engineering

CQV / Validation Experience

Education

Bachelor's Degree in Engineering, Science or related discipline

Tools

PLC Control Systems

PFD/P&ID Development

Job description

Katalyst CRO is seeking a Project Engineer in Illinois who will oversee medium size projects in the pharmaceutical sector. Responsibilities include capital project support, coordinating project scopes, managing equipment design, and ensuring compliance with GMP standards. The ideal candidate will have a Bachelor's Degree in Engineering, strong communication skills, and over four years of experience in a related field. This role requires technical knowledge of pharmaceutical equipment and project management expertise.