Computer system validation jobs in United States

The Analytical Equipment Validation (AEV) Specialist assesses changing analytical computer systems to ensure compliance with company policies and industry guidance. · ...

The Analytical Equipment Validation (AEV) Specialist, Level 3 assesses changing analytical computer systems to ensure compliance with company policies, procedures and industry guidance. · A ssess risk and implement a risk based approach to categorize computerized systems , change ...

We are seeking a CSV Engineer with strong DeltaV experience to support validation activities for automated systems in a GxP-regulated Life Sciences environment. · The ideal candidate will have hands-on experience in computer system validation, DeltaV DCS, · regulatory compliance ...

Computer system validation of SAP ERP system to meet GxP compliance. · ...

The Analytical Equipment Validation (AEV) Specialist, Level 3 assesses changing analytical computer systems to ensure compliance with company policies and industry guidance. · A ssess risk and implement a risk based approach to categorize computerized systems , change requests fr ...

We are seeking Computer System Validation Engineers with a strong focus on equipment-level validation. · Hands-on experience in equipment CSV ( manufacturing equipment control systems instruments) · Strong understanding of GxP regulations FDA 21 CFR Part 11 and validation best pr ...

Hiring for Computer System Validation (CSV) / Manufacturing Systems Engineer - Remote. · ...

This position involves reviewing and approving CSV lifecycle documents to ensure compliance with GAMP 5, 21 CFR Part 11, and Data Integrity principles. · Review and approve CSV lifecycle documents (VMP, URS, FRS) · ...

The CSV Engineer will lead and execute Computer System Validation (CSV) activities for GMP computerized systems supporting laboratory, manufacturing, and quality operations. · Lead CSV lifecycle activities including implementation, production support, change management. · ...

This role supports GMP-regulated manufacturing and laboratory operations through hands-on validation execution across equipment utilities facilities and processes You'll work closely with Engineering QA Manufacturing Facilities teams to ensure systems remain compliant qualified i ...

Review and approve CSV lifecycle documents (VMP, URS, FRS, HDS) to ensure risk-based validation approaches aligned with GAMP 5 and Data Integrity principles. · Evaluate system changes through change control assessing GxP impact and validation requirements. · ...

The Computer Systems Validation (Analytical Equipment), Specialist III assesses changing analytical computer systems to ensure compliance with company policies, procedures and industry guidance. · ...

Join us for a career full of opportunities where you can make a difference. · ...

This role supports GMP-regulated manufacturing and laboratory operations through hands-on validation execution across equipment, utilities, facilities, and processes. · <li_Execute IQ/OQ/PQ protocols for GMP-critical equipment including laboratory instruments, manufacturing equip ...

The Computer System Validation Specialist LES will develop and execute CSV deliverables for Lab Execution Systems as well as ensure the CSV strategy for Lab Execution Systems is applied to LES owned GxP and non-GxP applications throughout their operational lifecycle.4+ years expe ...

We are building a talent pool of candidates experienced in regulated industries for a Computer System Validation (CSV) Consultant position in Puerto Rico. · ...

The CSV Engineer will support Computer System Validation activities for GxP-regulated systems. This role involves executing validation deliverables and ensuring compliance with FDA guidelines. · ...

We're looking for a contract GxP / CSV Documentation &Validation Specialist to help clean up and finalize validation documentation for our software development workflow.. · This role is focused on post-merge review of GitHub pull requests and Jira tickets to ensure they meet our ...

We are seeking an experienced CSV professional to provide strategic and operational leadership for computerized systems across the pharmaceutical environment. · Lead and support multiple CSV projects using a risk-based approach. · Ensure validated systems remain compliant through ...

The Analytical Equipment Validation (AEV) Specialist, Level 3 assesses changing analytical computer systems to ensure compliance with company policies and industry guidance. · Lead end-to-end validation for analytical equipment as a Subject Matter Expert (SME), ensuring strict a ...