Senior CQV Validation Engineer – GMP Pharma

CAI; Greenville (NC); On-site; USD 85,000 - 125,000; Full time

Job summary

CAI in North Carolina seeks a CQV Engineer to lead commissioning, qualification, and validation activities in pharmaceutical projects, with a focus on safety and regulatory compliance.

You will coordinate testing with contractors, review CQV procedures, and help plan spares and resources across the project lifecycle. Willingness to travel within the U.S. required. CAI emphasizes integrity, teamwork and delivering critical solutions for regulated industries.

Qualifications

• BS/BA in Engineering, Chemistry, or Life Sciences; relevant experience may substitute for education.
• 3+ years in Pharmaceutical/Life Sciences.
• Experience in GMP environment.
• Strong written and oral communication.
• Willingness to travel across the U.S. and possibly internationally.

Responsibilities

• Perform CQV (Commissioning, Qualification, Validation) activities with a focus on safety.
• Deliver CQV tasks aligned to project schedules and document progress.
• Support creation and review of CQV procedures and qualification documents.
• Coordinate testing with project contractors and equipment vendors.
• Plan commissioning spares, consumables, and allocate resources.
• Assist with CQV reviews and qualification of equipment design.

Skills

Excellent communication

Problem solving

Customer-focused

Willingness to travel

Education

Bachelor’s degree in Engineering, Chemistry, or Life Sciences

Job description

CAI in North Carolina seeks a CQV Engineer to lead commissioning, qualification, and validation activities in pharmaceutical projects, with a focus on safety and regulatory compliance.

You will coordinate testing with contractors, review CQV procedures, and help plan spares and resources across the project lifecycle. Willingness to travel within the U.S. required. CAI emphasizes integrity, teamwork and delivering critical solutions for regulated industries.