A Validation Specialist tests and documents the validity and accuracy of manufacturing systems and equipment. Tests processes and manages process validations. Provides technical support and implements operating procedures. May create documentation to show that a manufacturing or production process has consistent results and meets quality standards.
CSV Specialist Katalyst Healthcares & Life Sciences - 4.0 Madison, WI Job Details Contract 1 day ago Qualifications Data integrity assurance GAMP Content creation for technical audiences Document control experience within pharmaceutical industry Pharmaceutical regulatory compliance
FDA 21 CFR
Part 11 Pharmaceutical company experience Biomedical regulatory compliance Test Execution (Quality assurance practices) Technical writing experience within technology Test validation method
Full Job Description Job Description:
We are seeking a CSV Specialist to support Computer System Validation (CSV) activities for GxP-regulated systems in the pharmaceutical, biotechnology, or medical device industry. The ideal candidate will be responsible for ensuring computerized systems are validated and compliant with regulatory requirements, company procedures, and industry standards.
Responsibilities:
Execute and support Computer System Validation (CSV) activities for GxP systems. Develop, review, and maintain validation documentation, including: Validation Plans User Requirements Specifications (URS) Functional Specifications (FS) Risk Assessments
IQ/OQ/PQ
Protocols Validation Reports Perform system impact assessments and risk-based validation activities. Support testing activities, including protocol execution and defect tracking. Ensure compliance with
FDA 21 CFR
Part 11, GAMP 5, GMP, and Data Integrity requirements. Collaborate with Business, IT, QA, and Engineering teams throughout the system lifecycle. Support change controls, deviations, CAPAs, and periodic reviews. Maintain validation records within electronic document management systems. Participate in internal audits and regulatory inspections.
Requirements:
Bachelor's degree in engineering, Computer Science, Life Sciences, Pharmacy, Biotechnology, or related field. 3+ years of CSV experience in a regulated pharmaceutical, biotechnology, or medical device environment. Knowledge of
GAMP 5, FDA 21 CFR
Part 11, GMP, and Data Integrity (ALCOA+) principles. Experience with validation documentation and testing activities. Familiarity with electronic quality management and document management systems. Strong technical writing and communication skills.
Preferred Qualifications:
Experience with CSA (Computer Software Assurance) methodologies.
Knowledge of systems such as:
TrackWise Veeva
SAP LIMS MES
Empower SharePoint ServiceNow Jira Experience supporting regulatory audits and inspections.
