CQV Validation Engineer — Pharma & Utilities

Cagents; Elkton (VA); On-site; USD 70,000 - 110,000; Full time

Job summary

CAI is a professional services company established in 1996 that delivers CQV and validation services for regulated industries worldwide. We are seeking a CQV engineer to develop documentation, write and execute field protocols, and summarize client-site activities.

The role focuses on pharmaceutical facilities, utilities, equipment, and project teamwork. Ideal candidates have 2–4 years' CQV experience and familiarity with ISPE Baseline Guide 5. Join CAI to drive excellence.

Qualifications

• Bachelor’s degree in a science or engineering field.
• 2–4 years’ experience in commissioning and qualification in a regulated industry.
• Familiarity with ISPE Baseline Guide 5 (Second Edition).
• Preferred experience: facilities/equipment startup, walk-downs, utilities, pharma processes.

Responsibilities

• Develop documentation for CQV activities.
• Write and execute protocols (field verification).
• Develop summary reports at client sites.
• Plan and coordinate work across small teams.
• Direct small teams in document development and/or execution.

Skills

CQV experience

ISPE Guide 5

Facilities startup

Education

Bachelor’s degree in science or engineering

Job description

CAI is a professional services company established in 1996 that delivers CQV and validation services for regulated industries worldwide. We are seeking a CQV engineer to develop documentation, write and execute field protocols, and summarize client-site activities.

The role focuses on pharmaceutical facilities, utilities, equipment, and project teamwork. Ideal candidates have 2–4 years' CQV experience and familiarity with ISPE Baseline Guide 5. Join CAI to drive excellence.