- 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
关于高知特 (Cognizant)
高知特(Cognizant)(纳斯达克代码:CTSH)作为一家AI Builder和相关技术服务提供商,致力于通过打造全栈AI解决方案,帮助企业将人工智能投资转化为实际价值。公司凭借深厚的行业经验、流程优化和工程技术专长,将企业独特的业务场景融入科技系统,赋能组织释放人才潜能,推动切实成果,并帮助全球企业在瞬息万变的环境中保持领先。如需了解更多详情,敬请访问 cognizant.ai 或关注@cognizant。
补充雇佣信息
薪酬信息截至本职位发布之日为准。Cognizant 保留在适用法律允许的范围内随时修改该信息的权利。
申请人可能需要通过现场面试或视频会议的方式参加面试。此外,候选人在每次面试时可能需要出示其当前所在州或政府签发的有效身份证件。
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