CSV Engineer
Katalyst HealthCares & Life Sciences
Job-ID32200742Reference26-00496Summary: IT CSV Validation Engineer is responsible for authoring and executing validation test scripts to support regulated systems within a GxP life sciences environment. This role will focus on validating ERP Master Data Governance processes and Data Lake platforms, ensuring compliance with regulatory requirements and data integrity standards.Roles & Responsibilities:Author, review, and execute validation test scripts (IQ/OQ/PQ) for GxP computerized systemsSupport validation activities for ERP Master Data Governance processes, ensuring data accuracy, integrity, and compliancePerform validation of Data Lake platforms and associated system interfaces, including data ingestion, transformation, and reporting layersCollaborate with cross-functional teams (IT, QA, Business, Data Engineering) to define validation scope, risk assessments, and acceptance criteriaEnsure compliance with GxP, 21 CFR Part 11, and data integrity requirements throughout the system lifecycleSupport deviation investigations, CAPAs, and change control activities related to validated systemsMaintain validation documentation including Validation Plans, Risk Assessments, Traceability Matrices, and Summary ReportsEducation & Experience:Bachelor's degree in Computer Science, Engineering, Life Sciences, or related discipline5+ years of Computer System Validation (CSV) experience in pharmaceutical or life sciences environmentsStrong experience with test script authoring and execution for GxP systemsExperience supporting Master Data Governance processes (SAP experience preferred but not required)Experience validating Data Lake environments and system interfaces (Snowflake experience preferred)Familiarity with AI/advanced data platforms is a plusExperience with validation management tools such as Val Genesis is a plusStrong understanding of GxP, 21 CFR Part 11, and data integrity principlesAbility to work independently and manage multiple validation activities with minimal oversight
- Requirements: Min 5 years of CSV experience. experience supporting validation of GxP GEN AI based solutions is a major plus experience supporting mergers/acquisitions/divestitures is a major plus Experience in the Pharmaceutical, biotechnology, or medical device industry...SuggestedRemote work
- ...Role - CSV Engineer Location - Raritan, NJ(Hybrid) Job Details: • 5-10 years' experience in Computer System Validation of GxP systems • Must have experience in Agile methodology and handled multiple releases in parallel • Extensive knowledge in CSV...SuggestedWork experience placement
- ...Job Summary: Shop Floor CSV/CSA Lead/Engineer responsible for leading and executing validation deliverables across the lifecycle in regulated manufacturing and laboratory GMP/GLP environments. The role includes automation/controls validation, risk-based validation...Suggested
$51 per hour
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...skills, and education among other factors. In addition, this position is eligible for an incentive bonus. The purpose of the Process Engineer's role will be to provide technical leadership to operate a major asset (typical annual revenue of $50MM to $200MM) at target...Full timeTemporary workFlexible hours- ...qualification activities and write detailed technical investigation reports for non-conformances. Partner closely with Maintenance, Engineering, Quality, and external vendors to ensure seamless installation and commissioning. Generate weekly and monthly validation...Immediate start
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