Computer System Validation (CSV) Engineer Pharma

Job Summary We are seeking a Validation Engineer with Computer System Validation (CSV) experience to support validation activities in a regulated pharma/biotech environment. The ideal candidate will have hands-on experience with validation lifecycles, GMP compliance, and documentation. Key Responsibilities Execute and support Computer System Validation (CSV) and equipment validation activities Develop and review validation plans, protocols (IQ/OQ/PQ), and reports Perform temperature mapping and validation studies Ensure compliance with GMP and regulatory requirements Handle deviations, CAPAs, and change control processes Support validation lifecycle activities including qualification and re-qualification Work cross-functionally with multiple teams and stakeholders Assist in audits and ensure documentation meets regulatory standards Required Qualifications 2-5 years of experience in Validation (CSV + Equipment/Utility/Facility) Strong understanding of GMP (Good Manufacturing Practices) Experience with: CSV (Computer System Validation) CAPA / Deviations / Change Control Data Integrity principles Experience in pharma, biotech, or life sciences industry Strong documentation and communication skills Preferred Skills Experience with aseptic processing or sterilization validation Knowledge of temperature mapping studies Ability to work independently with minimal supervision

Pay:

$44.00 - $45.00 per hour

Work Location:

In person