Validation Engineer
On-site · Boston, Massachusetts, United States or Providence, Rhode Island, United States
Job Summary
Validation Engineer responsible for developing documentation for CQV activities, writing and executing protocols (field verification), and developing summary reports at client sites. Focus areas include pharmaceutical facilities, utilities, and equipment. Project and team management duties include planning and coordinating work and directing small teams in document development and/or execution. Qualifications include a Bachelor’s degree in a science or engineering field (or equivalent experience) and 2–4 years’ experience in commissioning and qualification in a regulated industry; familiarity with ISPE Baseline Guide 5 is a plus; preferred experience in facilities and equipment startup, walk-downs and troubleshooting, utilities (WFI, RO, HVAC), upstream/downstream processing, purification, recovery, building automation, and pharmaceutical manufacturing processes.
Required Qualifications
- Bachelor’s degree in a science or engineering field (or equivalent experience)
- 2–4 years’ experience in commissioning and qualification in a regulated industry
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