What are the responsibilities and job description for the Systems Analyst - III position at Cube hub?
Job Title : Systems Analyst (GMP Pharma Industry FDA 21 CFR Part 11)
Job Location : Foster City California
job duration : 6 months
Job Description :
Hands on experience in setting up computers image network connections / setup windows infrastructure and configuration.
Solid understanding on Windows event logs functions and tools.
Should be able to resolve day to day issues encountered on lab computers connected to instruments.
Coordinate with corporate IT for their initiatives and implement same initiatives on Lab computers (Windows Patches Security Agents and network drop etc)
Manage inventory of lab computers and periodically checking if those computers are running fine and / or require any update.
Maintain existing GMP (Good Manufacturing Practices) standalone systems
Provide support during system audit trail review (Screenshots data & restore etc)
Manage vendors account on local computer
Perform periodic manual tasks as applicable
Taking image of computer workstation during decommissioning replacement and / or qualification
Support cross functional teams for their initiates (print driver installation security agents)
Issue Management Existing GMP Standalone Systems
L1 support on sparc tickets created for standalone systems.
Work with team for tracking and trending issues on standalone systems
Support team members for their requests on new computer setup local configurations validation of system decommissioning old computers taking an image and managing those images.
Support cross functionally for multiple initiatives that require changes in lab computers like driver installation local account / group / permission management.
Support lab personnel for issues regarding computer IT infrastructure and day today request regarding computerized systems in the lab.
Team player customer focused Critical thinking and problem solving skills are critical for this role
GMP & Compliance Knowledge (Regulated Lab Environments)
Understanding of Good Manufacturing Practices (GMP) and FDA 21 CFR Part 11
Experience with audit trail reviews data integrity and system validation
Managing GMP standalone systems while ensuring compliance with IT policies
Key Skills
Fund Management,Information Technology,Conveyancing Paralegal,Corporate Sales,Asic
Employment Type : Remote
Experience : years
Vacancy : 1
