Senior Validation Engineer - Pharma CQV Lead

CAI; Atlanta (GA); On-site; USD 90,000 - 130,000; Full time

Job summary

CAI is seeking a CQV engineer to execute commissioning, qualification, and validation activities in GMP environments. You will ensure CQV deliverables align with project schedules and safety standards, while tracking progress and coordinating with contractors and vendors for testing.

The role requires a bachelor's in engineering and 3+ years in pharma/Life Sciences, with strong communication skills and travel willingness across the U.S.

Qualifications

• Bachelor's degree in Engineering, Chemistry, or Life Sciences with GMP exposure.
• 3+ years of related experience in Pharmaceutical/Life Sciences.
• Essential GMP experience.
• Excellent communication skills.
• Willingness to travel within the U.S. and potentially internationally.

Responsibilities

• Perform CQV activities with a strong focus on safety.
• Deliver C&Q activities in alignment with project schedules.
• Track and report progress of CQV efforts.
• Support generation and review of CQV documentation and plans.
• Coordinate with project contractors and instrument vendors for testing.

Skills

CQV Execution

Validation

QA Documentation

Project Planning

Education

Bachelor’s degree in Engineering

Job description

CAI is seeking a CQV engineer to execute commissioning, qualification, and validation activities in GMP environments. You will ensure CQV deliverables align with project schedules and safety standards, while tracking progress and coordinating with contractors and vendors for testing.

The role requires a bachelor's in engineering and 3+ years in pharma/Life Sciences, with strong communication skills and travel willingness across the U.S.