Entry-Level Validation Engineer: Pharma CQV & Field Work

Doist; Columbus (OH); On-site; USD 55,000 - 75,000; Full time

Job summary

CAI is a professional services company delivering CQV documentation and field verification for pharmaceutical facilities and utilities. The role involves developing documentation, writing protocols, and producing client-site summary reports within cross-functional project teams.

Ideal candidates have 0–2 years of experience in any industry, a science or engineering background, and knowledge of ISPE Baseline Guide 5.

Qualifications

• Bachelor's degree in science or engineering preferred but not required.
• 0-2 years work experience in any industry.
• Familiarity with ISPE Baseline Guide 5 (Second Edition) is a plus.
• Preferred experience in facilities and equipment startup, walk-downs and troubleshooting, utilities, upstream/downstream processing, purification, recovery, building automation, and pharmaceutical manufacturing processes.

Responsibilities

• Develop documentation for CQV activities.
• Write and execute protocols (field verification).
• Develop summary reports at client sites.

Skills

CQV Documentation

Protocol Writing

Client Site Reporting

Project Coordination

Team Leadership

Regulatory Compliance

Education

Bachelor's degree in science or engineering (preferred)

0-2 years work experience

Tools

ISPE Baseline Guide 5 (Second Edition)

Job description

CAI is a professional services company delivering CQV documentation and field verification for pharmaceutical facilities and utilities. The role involves developing documentation, writing protocols, and producing client-site summary reports within cross-functional project teams.

Ideal candidates have 0–2 years of experience in any industry, a science or engineering background, and knowledge of ISPE Baseline Guide 5.