CAI
Validation Engineer
About this role
CAI seeks a Validation Engineer to support commissioning, qualification, and verification (CQV) activities at pharmaceutical and utility facilities. You'll develop technical documentation, execute field verification protocols, and lead small teams through complex qualification projects in highly regulated environments.
What you'll do
- Develop documentation and protocols for CQV activities at client sites
- Execute field verification work and produce summary reports
- Plan and coordinate validation projects across pharmaceutical facilities and equipment
- Direct small teams in document development and protocol execution
- Troubleshoot equipment and utilities (WFI, RO, HVAC) during facility startup
- Perform walk-downs and validate compliance with regulatory standards
What they're looking for
- Commissioning and qualification in regulated industries
- Technical documentation and protocol writing
- ISPE Baseline Guide 5 knowledge
- Pharmaceutical manufacturing processes
- Building automation and utilities systems
- Project planning and team coordination
- Problem-solving and troubleshooting
- Clear technical communication
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CAI
CAI provides commissioning, qualification, and validation services for pharmaceutical and life sciences facilities in regulated environments. The company is hiring Validation Engineers to lead CQV activities, develop technical documentation, execute verification protocols at client sites, and manage teams to ensure regulatory compliance and operational readiness.
View all jobs at CAILikely interview questions
- Describe your experience with CQV activities in a regulated pharmaceutical or utility environment.
- Walk us through how you would develop and execute a field verification protocol for a new piece of equipment.