C&Q Specialist

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

Current job opportunities are posted here as they become available.

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking C&Q Specialists to support equipment and systems in a biopharmaceutical facility. The specialists will execute field activities, document results, and work with project teams to complete system qualification.

• C&Q Specialist

Description:

• 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.

Qualifications:

• At least 5 years of C&Q experience in a pharmaceutical or biopharmaceutical facility.
• Experience with FAT, SAT, IQ, OQ, or comparable commissioning and qualification activities.
• Working knowledge of GMP requirements and controlled documentation.
• Strong field execution, technical writing, and teamwork skills.

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.

Excited to build something meaningful together? We look forward to hearing from you.

Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.