Senior Applications Administrator

Thermo Fisher Scientific

Senior Application Administrator responsible for administering laboratory middleware and instrument interfaces. Ensuring compliance with regulatory requirements and managing configurations in a GxP environment.

Posted 7/15/2026full-timeBangalore • 🇮🇳 IndiaSeniorWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in administering and supporting laboratory middleware applications, with a strong focus on configuration management, troubleshooting, and compliance in GxP-regulated environments. Proficient in executing Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) activities for laboratory information systems.

Highest-signal resume keywords

Laboratory Information Systems (LIS)Middleware Application SupportGxP-Regulated EnvironmentsInstallation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ)TCP/IP Networking

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Configuration ManagementTroubleshootingRoot Cause AnalysisChange ControlValidation DocumentationAudit SupportInstrument ManagerInterface TroubleshootingTest MappingCode Mapping

Tools & Technologies

Laboratory Middleware ApplicationsInstrument InterfacesCommunication ParametersDevelopment EnvironmentsTest EnvironmentsValidation EnvironmentsProduction Environments

Industry Keywords

Clinical Laboratory ScienceHealthcare ApplicationsMedical Device IntegrationManufacturing ApplicationsControlled Software Deployment Practices

Tech Stack

Tools & technologies

TCP/IP

About the role

Key responsibilities & impact

Administer and support laboratory middleware applications, including Instrument Manager and associated laboratory information systems (LIS)
Configure and maintain instrument interfaces, routing rules, test mappings, code mappings, and communication parameters
Manage application configurations across Development, Test, Validation, and Production environments
Perform troubleshooting and root cause analysis for interface failures, transmission issues, mapping discrepancies, and data integrity concerns
Execute and support Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) activities
Lead end-to-end testing activities for new and modified instrument interfaces

Requirements

What you’ll need

Bachelor's degree in Information Technology, Computer Science, Engineering, Medical Technology, Clinical Laboratory Science, or related discipline
5+ years of experience administering regulated laboratory, healthcare, clinical, or manufacturing applications
3+ years of experience supporting medical device, instrument, middleware, or laboratory system integrations
Experience working in GxP-regulated environments
Experience executing or supporting CSV activities including IQ, OQ, and PQ
Experience with change control, validation documentation, and audit support
Laboratory Information Systems (LIS) and middleware platforms
Instrument Manager or comparable middleware applications
TCP/IP networking, serial communications, and interface troubleshooting
Configuration management and controlled software deployment practices

Benefits

Comp & perks

Reasonable accommodation for individuals with disabilities in application and interview process
Employee benefits including health and safety programs