RL
CSV QA Lead
Resource Logistics, Inc.
🇺🇸 United States
Hybrid
Staff / Principal
1 week ago
- GxP
- AI
1 week ago
Not enough detail in this posting to match
Location - Raritan, NJ (Hybrid)
Rate - $55/hr w2
Must Have - Computer System Validation – validating GxP Gen AI Based systems
Job Summary • Candidates need to have hands-on experience in validating GxP GEN AI based solutions in Clinical space • Ability to manage multiple dispositions for multiple Pharmaceutical Managers with limited supervision. • Ability to manage end-end from Inventory, assessments, re,tions to final dispositions; 7-10 years of relevant experience; has experience of leading/advising Junior and Senior resources. Specifically in the Pharmaceutical, biotechnology, or medical device industry. • Experience in FDA and/or Global regulated environment with good understanding of GxP standards and Risk based validation; Define and implement Risk based validation activities. • Experience in writing and executing documentation for all aspects of the validation deliverables (etc. Requirements, Compliance/validation Plans, test protocols, Test Summary reports and Compliance/Validation Reports, SOPs/WIs). Experience in reviewing system test and user acceptance test scripts, Traceability matrix and Design Specs Experience in QA Methodologies, designing, reviewing and approving Test Plans, systems and UAT test scripts and Test procedures. • Strong verbal and written communication skills. • Ability to work as a team player, lead a team or accomplish tasks without supervision. • Ability to work with remote teams and support several changes/projects simultaneously. Ability to provide Validation guidance, timely reviews, and escalations to TQ management
CSV QA Lead · Resource Logistics, Inc.