| Validation Specialist - Raritan, NJ (Hybrid) - Contract at Raritan, New Jersey, USA |
| Email: [email protected] |
| From: Vijay Chepyala, Talent groups [email protected] Reply to: [email protected] Position: Validation Specialist Location:- Raritan, NJ (Hybrid) Duration:- Contract Must have: Computer System Validation, Quality Management System, Acquisitions and Mergers Keywords CSV, Computer System Validation, Tools validation, Quality Management System, 21 CFR 820, ISO 13485 , Acquisition, and mergers In addition to validation and regulation experience, the resource should have the following experience: Roles and Responsibilities Minimum 7 years Experience in the Validating IT software systems like Quality Management System in Life Sciences industry Experience in FDA and/or Global regulated environment with good understanding of GxP standards like CFR 820 and Risk based validation. Experience in validating Global Risk and Compliance modules. Provides consultation and counselling on Risk and Compliance module implementation in reference to regulatory quality. Knowledge of FDA guidances and industry standards 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) Experience in reviewing system test and user acceptance test scripts, Traceability matrix related to System data Archival process. Hands-on experience in software life-cycle management in System data archival process Ability to provide Validation guidance, timely reviews, and escalations to Project teams. Keywords: information technology New Jersey |
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| Wed Jan 24 22:49:00 UTC 2024 |