System Specialist
Core
Provide technical support for instrumentation lifecycle activities, including installation, configuration, maintenance, troubleshooting, and validation for cGMP instruments in Quality Control and Manufacturing environments.
Role type
System Specialist (Instrumentation Lifecycle)
Builds
Supports Quality Control and Manufacturing Instrumentation Programs
Domain
Life Sciences / Pharmaceutical Manufacturing / cGMP
Required skills
Hardware and software installation, configuration, and maintenance, Troubleshooting, Validation (IQ/OQ/PQ), System administration, Data integrity assessments, Electronic data reconciliation, Change control management, Project management
Preferred skills
cGMP principles and industry standards, Network technologies (VLAN, firewalls), Virtualization systems, Microsoft OS troubleshooting
Responsibilities
Support hardware and software installation, configuration, maintenance, and troubleshooting, Provide vendor and IQ/OQ/PQ support, Author and review validation and operation documentation, Resolve moderately complex instrumentation issues, Support system health checks and decommissioning
Seniority
Mid-level, hands-on IC
