Biopharma C&Q Specialist: Validation & Commissioning

Veg Group; New Albany (OH); On-site; USD 85,000 - 120,000; Full time

Job summary

Validation & Engineering Group, Inc. in the United States is seeking a C&Q Specialist to support biopharmaceutical equipment and systems. You will execute field activities, document results, and collaborate with project teams to complete qualification.

The role requires strong GMP knowledge, hands-on field execution, and proven ability to review drawings and vendor docs. Join a purpose-driven team delivering critical healthcare technology.

Qualifications

• Minimum 5 years of C&Q experience in pharma/biopharma facilities.
• Experience with FAT, SAT, IQ, OQ or similar qualification activities.
• Working knowledge of GMP requirements and controlled documentation.
• Strong field execution, technical writing, and teamwork skills.

Responsibilities

• Develop, review, and execute commissioning and qualification protocols.
• Perform field walkdowns, installation verification, and functional testing.
• Review drawings, specifications, and vendor documentation against installed systems.
• Document test results, investigate discrepancies, and support corrective actions.
• Coordinate with Engineering, Operations, and Quality to complete qualification and system turnover.

Skills

Field execution

Technical writing

Teamwork

Job description

Validation & Engineering Group, Inc. in the United States is seeking a C&Q Specialist to support biopharmaceutical equipment and systems. You will execute field activities, document results, and collaborate with project teams to complete qualification.

The role requires strong GMP knowledge, hands-on field execution, and proven ability to review drawings and vendor docs. Join a purpose-driven team delivering critical healthcare technology.