Lead, QCTS Data Integrity & Computerized Systems

About the role

The field of gene therapy is growing rapidly and Genezen is here to meet the exacting needs of our clients. We provide process development, produce GMP viral vectors, and provide cell transduction for gene and cell therapy clinical trials and are proud to be a part of the process that leads to new cures. WORKING AT GENEZEN Many people have worked in environments where you feel like just another nameless part of an enormous machine. Genezen is different. We want our employees to be innovative, collaborative problem solvers who are dedicated to meeting the challenges of working at a fast-growing company. We are dedicated to empowering our employees to be their best and making Genezen a rewarding place to work. Every employee contributes to the success of the company and you can be part of that team. JOB SUMMARY The Lead , Quality Control Technical Services (QCTS) - Data Integrity is responsible for ensuring that QC laboratory systems , instruments, software, and associated data workflows meet regulatory expectations for data integ rity and GxP compliance. This role provides expert oversight and support across QC laboratory for computerized system implementation, instrument qualification, assay data workflows, software validation , and data governance activities. The lead partners closely with QC operations, Validation, IT, and system owners to ensure that QC systems are designed and maintained, and monitored in alignment with 21 CFR Part 11 and EU Annex 11 , ALCOA+ prin ciples, and corporate data integrity standards . The role supports audits and inspections, authors technical documentation, resolves data-related issues, and contributes leadership through scientific and systems expertise . ESSENTIAL JOB FUNCTIONS Serve as the QCTS Data Integrity and Computerized System Validation SME, ensuring QC laboratory systems comply with 21 CFR part 11, EU Annex 11 and internal DI policies. Provide expertise and support for QC computerized systems, including instrument software, standalone ana lytical instruments, and data acquisition/proce ssing tools , including Excel spreadsheets . Partner with QC labs leads, system owners, Validation , and IT to ensure robust lifecycle management of QC systems, including system qualification, validation, periodic review, and configuration controls. Responsible for overall lifecycle management of computer system validation activities in QC/GMP environment. Lead implementation of change management of QC instruments, software upgrades, and new laboratory technologies to ensure readiness for GMP use. Maintain and improve data integrity practices within the QC function, including data review workflows, audit trails, user access, data storage, and backup/restore procedures. Support QC investigations (deviations, OOS/OOT, CAPAs) involving data integrity , system performance, or data workflow failures; provide technical root-cause contributions. Lead authoring and maintenance of QCTS procedures, work instructions , validation protocol, validation summary reports , and guidance documents relating to computerized systems, instrument qualification (IOQ, PQ) , and data integrity. Coordinate with external qualified service providers to ensure QC systems are validated . Support internal and external audits /inspections as the QCTS Data Integrity SME, providing evidence for QC systems, validation documentation, and data governance controls. Deliver training, guidance, and technical mentorship to QC analyst s and system users to strengthen data integrity awareness and consistent system usage across QC. SPECIAL JOB REQUIREMENTS Adaptability required as work schedule may change based on business needs Criminal background check required Other duties as assigned KNOWLEDGE, SKILLS AND EXPERIENCE EDUCATION / CERTIFICATIONS / LICENSES Degree in science-related field ON-THE-JOB EXPERIENCE 1 0 + years of experience in IT Systems/CSV, Enterprise Solutions ( Veeva , CDS ), QMS (electronic and paper), and data integrit y , Excel spreadsheet validation SKILLS / ABILITIES Prior experience working in a CDMO environment 10+ years working in a Good Manufacturing Practices (GMP) environment Subject matter expert in 21 CFR Part 11, GAMP 5 , EU A nnex 11 Subject matter expert in Good Documentation Practices (GDP) Excellent computer literacy (MS Word, Excel, Smart S heets ) Excellent project management tools (MS project, Smart S heets ) Excellent executive communication skill s , both written and oral Pay Range: The annual salary range for this position is $110,000-$150,000. PHYSICAL DEMANDS While performing the duties of this job, the employee is required to meet the following physical demands: Work Environment Regularly sit for long periods of time Movement Frequently required to stand; sit; use hands to finger, handle, or feel; reach with hands and arms Occasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawl Lifting Frequently lift and/or move up

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