- 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.
- 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.
- 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 readiness activities, and remediation programs.
- Familiarity with Jira, ServiceNow, or other IT service management and workflow platforms.
- Experience working within Agile delivery environments.
- Exposure to automation, AI-enabled support solutions, or digital transformation initiatives in laboratory operations.
- Medical/Dental/Vision/Life Insurance
- Paid holidays plus Paid Time Off
- 401(k) plan and contributions
- Long-term/Short-term Disability
- Paid Parental Leave
- Employee Stock Purchase Plan
About Cognizant
Cognizant (Nasdaq: CTSH) is an AI Builder and technology services provider, bridging the gap between AI investment and enterprise value by building full-stack AI solutions for our clients. Our deep industry, process and engineering expertise enables us to build an organization’s unique context into technology systems that amplify human potential, drive tangible outcomes and keep global enterprises ahead in a fast-changing world. See how at cognizant.ai or @cognizant.
Additional employment information
Compensation information is accurate as of the date of this posting. Cognizant reserves the right to modify this information at any time, subject to applicable law.
Applicants may be required to attend interviews in person or by video conference. In addition, candidates may be required to present their current state or government issued ID during each interview.
Cognizant is an equal opportunity employer. Your application and candidacy will not be considered based on race, color, sex, religion, creed, sexual orientation, gender identity, national origin, disability, genetic information, pregnancy, veteran status or any other characteristic protected by federal, provincial or local laws.










