Validation Engineer

Job summary: 5+ years of CQV experience focused on utilities, process equipment, and process validation. Strong documentation experience across CQV lifecycle deliverables including URS/FRS, risk assessments, protocols, summary reports, deviations, and trace matrices. Excellent technical writing and communication skills. Comfortable in a client-facing role with a professional demeanour. Strong team player working under a project lead. Preferred experience with equipment such as formulation vessels, non-sterile nasal spray fill lines, nasal sprayer assembly lines, inspection equipment, packaging and thermoforming equipment, and autoclaves.

Created: 2026-03-04