Data Integrity Specialist

Piper Companies is seeking a Data Integrity Specialist to support a leading pharmaceutical organization in developing and implementing site-level data integrity initiatives within a laboratory environment in Titusville, NJ. The Data Integrity Specialist will play a critical role in building data integrity frameworks, facilitating stakeholder collaboration, conducting risk assessments, and ensuring compliance with regulatory and quality standards. Responsibilities of the Data Integrity Specialist: Develop and execute Data Integrity (DI) risk assessments for laboratory systems, equipment, and processes. Create Level 3 process flow maps and facilitate working sessions with SMEs, vendors, and site stakeholders to identify and mitigate DI risks. Review existing risk assessments, compliance documentation, audit trails, periodic reviews, and other GxP-related records to identify gaps and improvement opportunities. Support configuration management activities for laboratory equipment and computerized systems while assisting with inspection readiness initiatives. Collaborate with teams to implement DI methodologies, communicate requirements, and support training initiatives across the organization. Qualifications of the Data Integrity Specialist: Experience supporting Data Integrity programs within a GMP-regulated pharmaceutical, biotechnology, or life sciences environment. Background in Computer System Validation (CSV) and familiarity with computerized systems used in laboratory settings. Working knowledge of 21 CFR Part 11, Annex 11, Good Documentation Practices (GDP), and GxP requirements. Experience reviewing technical documentation, audit trails, quality records, and compliance-related documentation. QC Laboratory, Stability Laboratory, internal auditing, or laboratory equipment experience is strongly preferred. Compensation for the Data Integrity Specialist includes: Pay Range: $55-$75 per hour (depending on experience) Comprehensive benefits package including medical, dental, vision, and retirement plans 15 month contract position This job opens for applications on 09/23/2026. Applications for this job will be accepted for at least 30 days from the posting date. SEO Keywords Data Integrity Consultant, Data Integrity Specialist, Computer System Validation, CSV Consultant, Data Integrity Risk Assessment, GMP Compliance, GDP Compliance, GxP Documentation, 21 CFR Part 11, Annex 11, Quality Assurance Consultant, Quality Systems, Audit Trail Review, Validation Specialist, Equipment Lifecycle Management, ELM, Pharmaceutical Compliance, Stability Laboratory, QC Laboratory, Laboratory Systems Validation, Technical Documentation, Inspection Readiness, Regulatory Compliance, Pharmaceutical Consultant, Data Review, Configuration Management, Life Sciences Consultant, Validation Engineer, Laboratory Compliance, Titusville NJ Jobs #LI-OG1 #LI-ONSITE #J-18808-Ljbffr