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Computer System Validation Consultant
Job in
Rahway, Union County, New Jersey, 07065, USA
Listed on 2026-06-22
Listing for:
Themesoft Inc.
Full Time
position Listed on 2026-06-22
Job specializations:
-
IT/Tech
IT QA Tester / Automation -
Quality Assurance - QA/QC
IT QA Tester / Automation
Job Description & How to Apply Below
- Experience/exposure to Computerized System Validation (CSV), US FDA 21 CFR Part 11, EU Annex 11 and GAMP 5.
- Experience of CSV Validation in any one of the Lab systems is must.
- Should worked in pharmaceutical domain and its related knowledge is must
- Good communication and technical writing skills are a must
- Developing validation documentation for pharmaceutical equipment, facilities and computerized systems used in GLP, GMP and GCP environments.
- Project Deliverables will encompass validation plans, specifications, test protocols and standard operation procedures and systems may include Process Automation, Laboratory Automation, Enterprise IT Applications and Network Infrastructure.
- CSV, GAMP 5 CPFR Part 11, Validation, Worked in V model, SOP & SDLC Lifecycle. Adaptation of CSA and Module Validation is preferred.
- To provide a planned approach for the implementation of the CSV deliverables, migration due diligence, GXP and Non GXP areas
- Provide guidance and leadership regarding Regulatory Compliance and Quality Management requirement.
- Prepare and execute URS, MVP, VP, RTM, TP, IQ, OQ, PQ, VSR, Traceability Matrix etc.
- Exposure to Regulatory Audits and Remediation activities
- Ensure the CSV artefacts are in line and meets regulatory requirements
- Preferred Experience in Agile Development
- Knowledge on working in Jira / Service Now
- Adaptation to AI is preferred.
- Experience in testing and knowledge in any one of the QC/R&D Lab systems is must.
- Prepare and execute TP, IQ, OQ, PQ, TSR, Traceability Matrix etc is must.
- Knowledge on working in Jira, HP ALM or any automation testing tools.
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