Sr Applications Administrator

Job Description :

Work Schedule

Environmental Conditions

Senior Application Administrator (Laboratory Systems & Medical Device Interfaces)

Job Summary

The Senior Application Administrator is responsible for administering, configuring, validating, and supporting Laboratory Information Systems (LIS), laboratory middleware, and medical device interfaces in a GxP-regulated environment. The role ensures compliant, reliable instrument integrations through Computer System Validation (CSV), data integrity, change control, and production support.

Key Responsibilities

• Administer and support LIS, Instrument Manager (or similar middleware), and laboratory interfaces.
• Configure instrument interfaces, test mappings, routing rules, and communication protocols (TCP/IP, serial, file-based).
• Execute Computer System Validation (IQ/OQ/PQ), validation documentation, and objective evidence.
• Perform End-to-End (E2E) testing and verify data integrity across instruments, middleware, and LIS.
• Manage change controls, impact assessments, system upgrades, and production deployments.
• Troubleshoot interface, mapping, and data transmission issues.
• Maintain audit-ready documentation and ensure compliance with GxP, 21 CFR Part 11, GDP, and ALCOA+.
• Collaborate with Laboratory Operations, QA, Validation, and IT teams.

Required Qualifications

• Bachelor's degree in IT, Computer Science, Engineering, Medical Technology, Clinical Laboratory Science, or related field.
• 5+ years supporting laboratory or regulated healthcare applications.
• 3+ years administering LIS, laboratory middleware, or medical device interfaces.
• Experience with GxP, CSV (IQ/OQ/PQ), change control, validation, and audit support.

Required Skills

• Laboratory Information Systems (LIS)
• Instrument Manager (or equivalent middleware)
• Medical device/instrument interfaces
• Computer System Validation (IQ/OQ/PQ)
• End-to-End Testing & Data Integrity
• Test mapping and configuration management
• Interface troubleshooting
• Change Control & Validation Documentation
• TCP/IP, serial communication
• Audit-ready documentation

Preferred Skills

• HL7/ASTM messaging
• GAMP 5
• Clinical laboratory or pharmaceutical domain experience
• Laboratory workflow, QC, and assay validation knowledge

Compliance Knowledge

21 CFR Part 11 . GxP . GLP . GCP . GDP . CSV . ALCOA+ . CAPA . Change Control

Key Competencies

Mandatory: IQ/OQ/PQ, E2E Testing, Data Integrity, Change Control, Objective Evidence.

Preferred: Test Mapping, Configuration Management, Interface Troubleshooting, Laboratory Workflow, Documentation Compliance, HL7, Instrument Manager, GAMP 5.

Working Hours:

India: 01:00 PM to 10:00 PM IST

Philippines: 03:30 PM to 12:30 AM PHT