| CSV Consultant at Raritan, New Jersey, USA |
| Email: [email protected] |
| From: Gunjan, Intellectt [email protected] Reply to: [email protected] Job role: CSV Consultant Location: Raritan, NJ(Hybrid) Duration: Contract Responsibility: Experience in the Pharmaceutical, industry 8+ years experience with System Development Lifecyle Experience in FDA and/or Global regulated environment with good understanding of GxP standards and Risk based validation. In Clinical Space Knowledge of FDA guidance s and industry standards (i.e., GAMP) Experience in writing and executing documentation for all aspects of the validation deliverables like 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 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 Technology Quality management. Keywords: quality analyst New Jersey CSV Consultant [email protected] |
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| Wed Aug 21 03:04:00 UTC 2024 |