IT Quality Validation Consultant / Computer System Validation Consultant
No H1B and/or C2C Please!!Job Title:
IT Quality Validation Consultant / Computer System Validation Consultant (Pharma/Biotech)W2 Contract & Hybrid role Work Location:
Nutley, NJOne of our leading Pharmaceutical client is looking for an IT Quality Validation Consultant / Computer System Validation Consultant, who will Prepare computer validation documents such as Validation Plans, User Requirements, Configuration Specifications, Test Protocols, and Summary Reports. Prepare Change Control documentation. Required Skill &
Experience:
BS Degree IN Technical field and extensive Pharmaceutical experience. 5-7 years experience in writing IT system validation protocols including IQs/OQs/PQs, project summary report. Deep understanding of SDLC and IT/system change management processes. Experienced in writing system implementation project related documentation such as project charter, implementation plan, communication plan, risk management plan.
Responsibilities:
Prepare Change Control documentation. Execute test scripts. Perform risk assessments. Must be familiar with 21 CFR Part 11. Prepare Project Plans. BS in a technical field and 5 years experience in GxP environment. Recommended Skills Change Management Communication Pharmaceuticals Project Charter Risk Analysis Risk Management Apply to this job. Think you're the perfect candidate? Apply on company site $(document).ready( function() $(#ads-desktop-placeholder).html(
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n Estimated Salary: $20 to $28 per hour based on qualifications.
IT Quality Validation Consultant / Computer System Validation Consultant (Pharma/Biotech)W2 Contract & Hybrid role Work Location:
Nutley, NJOne of our leading Pharmaceutical client is looking for an IT Quality Validation Consultant / Computer System Validation Consultant, who will Prepare computer validation documents such as Validation Plans, User Requirements, Configuration Specifications, Test Protocols, and Summary Reports. Prepare Change Control documentation. Required Skill &
Experience:
BS Degree IN Technical field and extensive Pharmaceutical experience. 5-7 years experience in writing IT system validation protocols including IQs/OQs/PQs, project summary report. Deep understanding of SDLC and IT/system change management processes. Experienced in writing system implementation project related documentation such as project charter, implementation plan, communication plan, risk management plan.
Responsibilities:
Prepare Change Control documentation. Execute test scripts. Perform risk assessments. Must be familiar with 21 CFR Part 11. Prepare Project Plans. BS in a technical field and 5 years experience in GxP environment. Recommended Skills Change Management Communication Pharmaceuticals Project Charter Risk Analysis Risk Management Apply to this job. Think you're the perfect candidate? Apply on company site $(document).ready( function() $(#ads-desktop-placeholder).html(
n
n
n Estimated Salary: $20 to $28 per hour based on qualifications.
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