> Markdown version of [/jobs/ext/3961704-csv-engineer](https://www.wearedevelopers.com/jobs/ext/3961704-csv-engineer). Every page supports `.md` or `Accept: text/markdown`. Links point to the HTML versions so they work for humans too. Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # CSV Engineer - **Company:** Katalyst Talent Agency - **Location:** Indianapolis, IN, United States - **Experience:** Expert - **Contract:** Permanent contract - **Skills:** Data Integrity, System Testing, Iq/oq/pq, Computerised Systems, Information Technology - **Published:** October 27, 2026 - **Apply:** https://www.careerbuilder.com/job-details/csv-engineer-indianapolis-in--e1046d15-86d8-4443-83a9-6bd01c3ecad3 ## About the Role * Approximately 5 10 years of validation experience within pharmaceutical, biotechnology, biopharmaceutical, or another GMP-regulated environment. * Strong Computer System Validation experience. * Experience supporting validation of GMP computerized systems. * Working knowledge of the CSV lifecycle, including validation planning, requirements, risk assessment, testing/protocol execution, traceability, and validation documentation. * Understanding of data integrity and GMP expectations for computerized systems. * Equipment validation / CQV experience in addition to CSV. * Ability to execute established validation protocols and clearly document results. * Experience investigating and documenting validation discrepancies or execution issues. * Ability to work cross-functionally with Quality, Engineering, Automation, Manufacturing, IT, and system owners. * ValGensis is a plus. ## Description * Seeking experienced CSV Engineers to provide onsite validation support within a regulated biopharmaceutical manufacturing environment. * The primary focus of the position will be Computer System Validation, while also supporting equipment qualification and broader CQV activities as project priorities require. * Consultants will support validation documentation and execution activities, assess computerized systems against GMP requirements, execute approved validation protocols, document test results, investigate discrepancies, and work cross-functionally with Engineering, Quality, Manufacturing, Automation, IT, and system owners. * Candidates should be comfortable supporting multiple validation workstreams and working independently in a fast-moving project environment.