C&Q Specialist/Engineer in Pharma & Life Sciences Validation

Veg Group; Town of Texas (WI); Hybrid; USD 90,000 - 120,000; Full time

Job summary

Validation & Engineering Group, Inc. seeks a Commissioning & Qualification (C&Q) Specialist / Engineer to join our life sciences team.

The role supports commissioning, qualification, and validation activities for equipment, utilities, facilities, systems, and processes. The successful candidate will develop and execute IQ/OQ/PQ protocols and related documents, work cross-functionally with Engineering, Quality, Validation, Manufacturing, Automation, and Project Management, and ensure

Qualifications

• Bachelor's degree in Engineering, Life Sciences, or related technical field.
• 3+ years of experience in commissioning, qualification, validation, or related field.
• Experience in pharmaceutical, biotech, GMP-regulated environments.
• Knowledge of IQ/OQ/PQ, FAT/SAT, risk assessments, and validation documentation.

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 equipment/system startup, troubleshooting, testing, and turnover.
• Work with Engineering, Quality, Validation, Manufacturing, Automation, and Project Management teams.
• Ensure activities comply with GMP, FDA, ISO, and applicable industry standards.
• Support deviations, change controls, and other project documentation as needed.

Skills

Technical writing

Communication

Problem solving

Cross-functional teams

Education

Bachelor's degree in Engineering or Life Sciences

Job description

Validation & Engineering Group, Inc. seeks a Commissioning & Qualification (C&Q) Specialist / Engineer to join our life sciences team.

The role supports commissioning, qualification, and validation activities for equipment, utilities, facilities, systems, and processes. The successful candidate will develop and execute IQ/OQ/PQ protocols and related documents, work cross-functionally with Engineering, Quality, Validation, Manufacturing, Automation, and Project Management, and ensure