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Sr. Lab Computing Support Engineer

Job in Raritan, Somerset County, New Jersey, 08869, USA
Listing for: Cognizant
Full Time position
Listed on 2026-09-27
Job specializations:
  • IT/Tech
Salary/Wage Range or Industry Benchmark: 80000 - 105000 USD Yearly USD 80000.00 105000.00 YEAR
Job Description & How to Apply Below

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.

"Please note, this role is not able to offer visa transfer or sponsorship now or in the future."

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 Service Now, 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 FDA 21 CFR Part 11, GAMP 5, and CSV best practices.
  • Experience supporting laboratory system onboarding, offboarding, configuration management, and data archival processes.
  • Experience participating in regulatory inspections, audit…
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