Validation Engineer – Pharma CQV & Systems

Caiready; Sacramento (CA); On-site; USD 85,000 - 120,000; Full time

Job summary

CAI in Sacramento is seeking a qualified CQV professional to develop documentation for commissioning and qualification activities in regulated environments. You will write and execute field protocols, develop and assemble data-rich CQV packages, coordinate client-facing activities, and deliver clear summary reports at client sites with accuracy and timeliness.

Ideal candidates hold a bachelor’s degree in science or engineering and have 2–4 years’ experience in commissioning and qualification

Qualifications

• Bachelor’s degree in science or engineering (or equivalent).
• 2–4 years’ experience in commissioning and qualification in a regulated industry.
• Familiarity with ISPE Baseline Guide 5 (Second Edition) is a plus.
• Preferred experience in facilities and equipment startup.
• Walk-downs and troubleshooting experience.
• Utilities (WFI, RO, HVAC) experience.
• Upstream/downstream processing and pharmaceutical manufacturing knowledge.

Responsibilities

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

Skills

CQV documentation

Protocol writing

Client liaison

Education

Bachelor’s degree in science or engineering

Job description

CAI in Sacramento is seeking a qualified CQV professional to develop documentation for commissioning and qualification activities in regulated environments. You will write and execute field protocols, develop and assemble data-rich CQV packages, coordinate client-facing activities, and deliver clear summary reports at client sites with accuracy and timeliness.

Ideal candidates hold a bachelor’s degree in science or engineering and have 2–4 years’ experience in commissioning and qualification