Pharma CQV Validation Engineer

CAI; Marietta (PA); On-site; USD 73,000 - 80,000; Full time

Benefits offered by this job

Comprehensive Health Insurance

24 days of Paid Time Off

Company paid Life Insurance

Company paid Long Term Disability

Job summary

CAI is a professional services firm seeking a CQV engineer with 2–4 years in commissioning in regulated environments to develop CQV documentation, write field verification protocols, and generate client-ready summaries.

You will plan activities, coordinate teams, and help validate facilities, utilities, and equipment across pharmaceutical projects, with growth opportunities within a global company.

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) is a plus.
• Experience in facilities and equipment startup; walk-downs and troubleshooting; utilities (WFI, RO, HVAC); upstream/downstream processing; purification, recovery; building automation; pharmaceutical manufacturing processes.

Responsibilities

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

Skills

CQV documentation

Field verification

Team leadership

Project coordination

Education

Bachelor’s degree in science/engineering

2–4 years commissioning experience

Job description

CAI is a professional services firm seeking a CQV engineer with 2–4 years in commissioning in regulated environments to develop CQV documentation, write field verification protocols, and generate client-ready summaries.

You will plan activities, coordinate teams, and help validate facilities, utilities, and equipment across pharmaceutical projects, with growth opportunities within a global company.