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Cognizant
Lab Computing Support Specialist
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What they do
A Validation Specialist tests and documents the validity and accuracy of manufacturing systems and equipment. Tests processes and manages process validations. Provides technical support and implements operating procedures. May create documentation to show that a manufacturing or production process has consistent results and meets quality standards.
$103,608 / year median in New Jersey
+5% projected growth
Job Description
"Please note, this role is not able to offer visa transfer or sponsorship now or in the future." As a Lab Computing Support Specialist , you will make an impact by ensuring the reliability, compliance, and operational excellence of laboratory systems that support research, quality, and manufacturing activities within a regulated Life Sciences environment. You will be a valued member of the Laboratory Informatics and IT team and work collaboratively with laboratory scientists, quality assurance, validation, infrastructure, application support, and business stakeholders to maintain compliant and efficient laboratory operations. In this role, you will: Manage the lifecycle of laboratory systems, including implementation, validation, maintenance, upgrades, patching, backup, archival, and decommissioning activities. Provide technical support for laboratory software systems, instrument integration platforms, and analytical instruments while troubleshooting software, hardware, and connectivity issues. Partner with laboratory, QA, and IT teams to ensure compliance with GxP, GLP, GMP, Computer System Validation (CSV), and data integrity requirements. Coordinate with vendors for system installations, maintenance, upgrades, issue resolution, and service management while ensuring compliance with regulatory and operational requirements. Support audits, inspections, change management, deviation management, CAPA activities, documentation updates, and continuous improvement initiatives across laboratory systems. Work model At Cognizant, we strive to provide flexibility wherever possible, and we are here to support a healthy work-life balance through our various well-being programs. Based on this role's business requirements, this is an onsite position requiring 5 days per week in a client office in Spring House, Pennsylvania. The working arrangements for this role are accurate as of the date of posting. This may change based on the project you're engaged in, as well as business and client requirements. Rest assured; we will always be clear about role expectations. What you need to have to be considered Bachelor's degree in Life Sciences, Information Technology, Engineering, Computer Science, or a related discipline. Experience supporting laboratory systems within pharmaceutical, biotechnology, or other regulated Life Sciences environments. Strong understanding of GxP, GLP, GMP, data integrity principles, and regulatory requirements. Hands-on experience with Computer System Validation (CSV), SDLC, and validation lifecycle activities. Experience supporting laboratory software applications, analytical instruments, and instrument integration platforms. Knowledge of laboratory workflows and familiarity with analytical instruments such as HPLC, GC, spectrophotometers, or similar laboratory technologies. Experience with user administration, backup and recovery processes, software upgrades, patch management, and system maintenance activities. Working knowledge of ticketing and service management tools such as ServiceNow, Remedy, or similar platforms. Experience with deviation management, change control, CAPA processes, and audit support activities. Strong troubleshooting, communication, technical documentation, and stakeholder management skills. These will help you stand out Experience supporting regulated laboratory environments within pharmaceutical research, development, manufacturing, or quality operations. Knowledge of Computer System Validation deliverables and regulatory frameworks including