Senior Data Integrity Consultant

Senior Data Integrity Consultant Avispa Technology - 4.8 San Diego, CA Job Details Temporary | Full-time | Contract $92 an hour 13 hours ago Benefits Dental insurance Vision insurance Qualifications GAMP Technical documentation Pharmaceutical regulatory compliance Quality management Data quality management Technical writing FDA regulations Training delivery Full Job Description Senior Data Integrity Consultant

ROCGJP00040531

Hourly pay: $92/hr

Worksite:

Leading biotechnology company (San Diego, CA 92111 - Onsite) W2 Employment, Group Medical, Dental, Vision, Life, Retirement Savings Program, PSL 40 hours/week, 6 Month Assignment A leading biotechnology company is seeking a Senior Data Integrity Consultant to lead and oversee Data Integrity (DI) and Computer System Validation (CSV) initiatives within a clinical-stage manufacturing environment. This role will provide Quality oversight of computerized systems, ensuring data accuracy, security, and compliance with global regulatory standards to support cell and gene therapy development.

Senior Data Integrity Consultant Responsibilities:

Lead the deployment and continuous improvement of the site's Data Integrity program, conducting gap assessments, developing mitigation plans, and ensuring compliance with FDA (21 CFR Part 11/210/211/820), EU Annex 11, ALCOA+ principles, and global quality standards. Provide Quality oversight for computerized systems and SDLC documentation (URS, design specs, test plans), ensuring data governance, audit trails, security controls, and system architecture meet regulatory and internal requirements. Author, review, and approve validation deliverables (IQ/OQ/PQ, validation plans, risk assessments, summary reports), support system requalification and periodic reviews, and guide project teams through compliant system lifecycle execution. Drive operational compliance through activities such as periodic system reviews, user access reviews, and change control oversight, while leading or supporting internal/external audits and regulatory inspections (FDA/EMA) and managing CAPA and risk mitigation efforts. Collaborate cross-functionally to enhance quality systems and procedures, support integration of local and global standards, provide expert consultation on data and system challenges, deliver training on DI/CSV practices, and prepare reports on compliance status and system performance.

Senior Data Integrity Consultant Qualifications:

8+ years of experience in a GxP-regulated environment (pharma, biotech, or cell/gene therapy), with a strong focus on Data Integrity, CSV, and Quality Compliance. Bachelor's degree in Life Sciences, Engineering, Computer Science, or related field (or equivalent experience). Expert knowledge of FDA regulations (21 CFR Part 11, 210/211/820), EU Annex 11, EudraLex Volume 4, GAMP 5, and ALCOA+ data integrity principles. Hands-on experience with Quality Management Systems (QMS), including Change Control, Deviations, CAPA, Document Control, Training systems, and electronic systems (EDMS, LMS, lab/manufacturing platforms). Strong technical writing, communication, and analytical skills, with the ability to manage multiple projects, work independently, deliver training, and support audits in a fast-paced environment.

Shift:

8:00 am to 5:00 pm. May need to have some flexibility to work earlier/later as needed. (H)