Computer System Validation Engineer
Job in
New Wilmington, Lawrence County, Pennsylvania, 16142, USA
Listed on 2026-10-14
Listing for:
Katalyst CRO
Full Time
position Listed on 2026-10-14
Job specializations:
-
Quality Assurance - QA/QC
Regulatory Compliance Specialist, QA Specialist - Analyst/Manager
Job Description & How to Apply Below
- Experienced CSV (Computer System Validation) Consultant with expertise in GxP-compliant environments to support validation, compliance, and audit readiness across life sciences systems.
- Strong experience in CSV processes, regulatory frameworks, validation documentation, and exposure to clinical and regulatory domains.
- Perform Computer System Validation (CSV) activities aligned with 21 CFR Part 11 / 820, GxP, GAMP 5, SOX, EU Annex 11 / Annex 22, ISO 9001, and ITIL.
- Ensure audit and inspection readiness.
- Conduct periodic reviews, access roster reviews, and audit trail reviews.
- Manage deviations, CAPA processes, SOP, and policy compliance.
- Author and review URS / FS documents, validation protocols, validation plans & reports, and final summary reports.
- Perform risk-based validation and testing aligned with CSA (Computer Software Assurance).
- Support validation lifecycle from planning to execution and closure.
- Work with platforms such as Veeva Vault Suite, Lab Ware LIMS, SAP (GxP modules), and BIOVIA Electronic Lab Notebook.
- Collaborate with teams across Biostatistics, Clinical & Discovery, Medical Affairs, Pharmacovigilance, Regulatory Affairs, Manufacturing, Quality, and Tech Ops.
- Experienced CSV (Computer System Validation) Consultant with expertise in GxP-compliant environments to support validation, compliance, and audit readiness across life sciences systems.
- Strong experience in CSV processes, regulatory frameworks, validation documentation, and exposure to clinical and regulatory domains.
- Perform Computer System Validation (CSV) activities aligned with 21 CFR Part 11 / 820, GxP, GAMP 5, SOX, EU Annex 11 / Annex 22, ISO 9001, and ITIL.
- Ensure audit and inspection readiness.
- Conduct periodic reviews, access roster reviews, and audit trail reviews.
- Manage deviations, CAPA processes, SOP, and policy compliance.
- Author and review URS / FS documents, validation protocols, validation plans & reports, and final summary reports.
- Perform risk-based validation and testing aligned with CSA (Computer Software Assurance).
- Support validation lifecycle from planning to execution and closure.
- Work with platforms such as Veeva Vault Suite, Lab Ware LIMS, SAP (GxP modules), and BIOVIA Electronic Lab Notebook.
- Collaborate with teams across Biostatistics, Clinical & Discovery, Medical Affairs, Pharmacovigilance, Regulatory Affairs, Manufacturing, Quality, and Tech Ops.
- 8-10 years of experience in Computer System Validation (CSV).
- Strong knowledge of GxP regulations, validation frameworks, GAMP 5, and CSA principles.
- Experience with CAPA, deviation management, SOP, and policy compliance.
- Strong documentation and validation lifecycle experience.
- Good understanding of life sciences domain processes.
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
Search for further Jobs Here:
×