Packaging Automation C&Q Specialist – Biopharma

Veg Group; Beloit (OH); On-site; USD 90,000 - 130,000; Full time

Job summary

Validation & Engineering Group, Inc. seeks a CQ Specialist for Packaging Automation to support commissioning, qualification, and related activities in a biopharmaceutical environment.

The role collaborates with Engineering, Automation, Operations, and Quality to bring systems into service and ensure compliance. Responsibilities include developing and executing qualification protocols, supporting startup and testing, reviewing requirements, and maintaining GMP-compliant documentation.

Qualifications

• At least 5 years of relevant C&Q experience in a pharmaceutical or biopharmaceutical environment.
• Hands-on experience with packaging equipment and automated controls, including PLC/HMI systems.
• Experience with FAT, SAT, IQ, OQ, and related qualification activities.
• Strong technical writing, troubleshooting, and cross-functional communication skills.

Responsibilities

• Develop, review, and execute commissioning and qualification protocols for packaging equipment and associated automation systems.
• Support equipment startup, functional testing, and troubleshooting.
• Review system requirements, drawings, specifications, and test results to confirm that equipment performs as intended.
• Document test results, investigate discrepancies, and support their resolution.
• Maintain clear, complete documentation in accordance with GMP requirements.

Skills

CQ experience

Technical writing

Cross-functional communication

Tools

PLC/HMI

Qualification protocols

Job description

Validation & Engineering Group, Inc. seeks a CQ Specialist for Packaging Automation to support commissioning, qualification, and related activities in a biopharmaceutical environment.

The role collaborates with Engineering, Automation, Operations, and Quality to bring systems into service and ensure compliance. Responsibilities include developing and executing qualification protocols, supporting startup and testing, reviewing requirements, and maintaining GMP-compliant documentation.