computer system validation

Job DescriptionAll the relevant skills, qualifications and experience that a successful applicant will need are listed in the following description.Requirements:Ands-on experience executing relevant lab CSV activities.Ensuring validation and ongoing compliance of laboratory validation and instruments.Data integrity, laboratory systems, testing, and CSV...

Computer System Validation Tester with Audit For further information about this role please contact: Nic Pietrantonio, Deputy Pathology CSV Lead, Nic.Pietrantonio@esneft.nhs.uk Interview date: 20th November Working at ESNEFT We pride ourselves on supporting our staff. We offer a wide range of training and development opportunities, as well as flexible...

Consultant–Computer System Validation-Life Sciences Indianapolis, IN, New York, NY, Somerset, NJ State / Region / Province Indiana, New Jersey, New York Country USA Skills Domain Consulting Interest Group Company ITL USA Requisition ID 155670BR Salary min 84706 Salary max 102941 Consultant, Business Consulting – Computer System...

Quality & Compliance Manager, Computer System Validation Remote, United States JOB SUMMARY The Quality & Compliance Manager, Computer System Validation manages the quality oversight and lifecycle validation of GxP computerized systems supporting CRO and laboratory operations. The role partners with Quality, IT, system owners, operational teams, and external...

Qualcomm Technologies, Inc. in San Diego, CA, is seeking a senior-level engineer to advance end-to-end system validation for SoCs. The role focuses on content quality, system-level validation enablement, and collaborative debugging across hardware and software boundaries. The ideal candidate will work on AI accelerators, memory subsystems, and silicon...

Qualcomm Technologies, Inc. in San Diego, CA, is seeking a senior-level engineer to advance end-to-end system validation for SoCs. The role focuses on content quality, system-level validation enablement, and collaborative debugging across hardware and software boundaries. The ideal candidate will work on AI accelerators, memory subsystems, and silicon...

Planet Pharma is seeking a validation SME to support validation of computerized systems, equipment, and instruments (systems). The role includes change control, data integrity assessments, and periodic review to ensure compliance with regulatory expectations.You will define validation requirements, coordinate risk assessments, and manage test protocols (OQ,...

Role: Data Validation Specialist (Remote) Location: Remote — United States & Canada Only Engagement Type: Hourly Contract Applicants must currently reside in and be authorized to work in the United States or Canada. Overview We are looking for a Data Validation Specialist to evaluate AI-generated content and data for accuracy, consistency, completeness,...

Katalyst-Healthcares- in Newark, CA seeks an experienced Computer Systems Validation Specialist to lead validation efforts for computerized systems, ERP, LIMS, and MES within a highly regulated life sciences environment. You will develop validation strategies, write protocols, and coordinate OQ/UAT testing across IT, engineering, QA, and manufacturing...

Qualcomm Technologies, Inc. in San Diego, CA, is seeking a senior-level engineer to advance end-to-end system validation for SoCs. The role focuses on content quality, system-level validation enablement, and collaborative debugging across hardware and software boundaries. The ideal candidate will work on AI accelerators, memory subsystems, and silicon...

Quality Chemical Laboratories (QCL), a leading Pharmaceutical testing and manufacturing laboratory in Wilmington, is seeking a qualified candidate for the position of Computer System Validation Specialist. Responsibilities: Performs and leads computer system validation projects related to authoring and executing validation documentation for laboratory...

Company Qualcomm Technologies, Inc. Job Area Engineering Group, Engineering Group > ASICS Engineering About the Team Qualcomm’s System Validation & Emulation (SVE) team is part of the central SoC validation organization responsible for ensuring end-to-end silicon quality across pre- and post-silicon phases. This role focuses on content quality and...

Veeva Systems, Inc. is seeking a Director of Computer Systems Validation to lead and mentor multi-site teams ensuring compliance with GMP, GCP, and quality standards.The role focuses on validation of Veeva Vault and internal systems, with emphasis on risk-based approaches, automation, and AI-driven capabilities. You will collaborate with Product Development,...

Our client, a leading organization in the pharmaceutical industry, is seeking a dedicated QA Validation Specialist to join their team.As a QA Validation Specialist, you will be part of the Quality Assurance department supporting validation and compliance initiatives.The ideal candidate will demonstrate attention to detail, proactive problem-solving skills,...

Computer System Validation (CSV) Specialist – ConsultantLocation: Remote with preference for 1–2 days onsite per week in the greater Cincinnati, Ohio area.Schedule: Part-time, approximately 20 hours per weekDuration: 3 monthsStart: ASAPPosition OverviewWe are seeking an experienced Computer System Validation (CSV) Specialist to support the remediation of...

A biopharmaceutical organization is seeking an experienced Computer Systems Validation Specialist to support business-application implementation projects and ongoing system changes. This position will provide CSV strategy, validation documentation leadership, and project-level coordination to ensure computerized systems are implemented and maintained in...

Job DescriptionSenior Consultant, Business Consulting – Computer System Validation- Life SciencesWe are looking for smart, self-driven, high-energy people with intellectual curiosity and passion for excellence; specifically, we are looking for candidates at Senior Consultants levels who are experienced in IT Computerized System Validation (CSV) within Life...

Precision Medicine Group is looking for a Quality & Compliance Manager, Computer System Validation to oversee the lifecycle validation of GxP computerized systems across CRO and laboratory operations. This role partners with Quality, IT, system owners, and vendors to ensure data integrity and inspection readiness from implementation through...

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing...

Job DescriptionJob DescriptionECHO Consulting Group is a leader in providing solutions for the pharmaceutical, biotechnology, medical devices, and food industries. ECHO Consulting Group delivers high-quality solutions in CQV, quality management, regulatory compliance, manufacturing support, and project management. We are committed to offering exciting career...