C&Q Engineer - Life Sciences (GMP)

Veg Group; North Carolina; On-site; USD 85,000 - 110,000; Full time

Job summary

Validation & Engineering Group, Inc. seeks a Commissioning & Qualification Specialist/Engineer to support C&Q activities across equipment, utilities, facilities, systems, and processes within regulated life sciences environments.

You will develop and execute IQ/OQ/PQ protocols, perform risk assessments, and collaborate with Engineering, Quality, Validation, Manufacturing, and Automation teams to ensure GMP-compliant turnover and documentation.

Qualifications

• Bachelor's degree in Engineering, Life Sciences, or related field preferred.
• 3+ years of experience in commissioning, qualification, validation, engineering, or related field.
• Experience in pharmaceutical, biotech, medical device, or GMP-regulated environments.

Responsibilities

• Support commissioning, qualification, and validation activities for equipment, utilities, facilities, systems, and processes.
• Develop, review, and execute C&Q documentation, including URS, risk assessments, FAT/SAT, IQ/OQ/PQ, protocols, and reports.
• Support deviations, change controls, and other project documentation as needed.
• Work closely with Engineering, Quality, Validation, Manufacturing, Automation, and Project Management teams.

Skills

Cross-functional collaboration

Technical writing

GMP/regulated environments

Problem-solving

Education

Bachelor's degree in Engineering, Life Sciences, or related technical field

Tools

IQ/OQ/PQ

FAT/SAT

Job description

Validation & Engineering Group, Inc. seeks a Commissioning & Qualification Specialist/Engineer to support C&Q activities across equipment, utilities, facilities, systems, and processes within regulated life sciences environments.

You will develop and execute IQ/OQ/PQ protocols, perform risk assessments, and collaborate with Engineering, Quality, Validation, Manufacturing, and Automation teams to ensure GMP-compliant turnover and documentation.