| Hiring for CSV Validation Lead - Raritan, NJ (Hybrid) at Raritan, New Jersey, USA |
| Email: [email protected] |
| From: Kowsalya.a, IDC [email protected] Reply to: [email protected] Hello Hope you are doing Great We have an urgent opening of CSV Validation Lead - Raritan, NJ (Hybrid) Contract role with our client, kindly read the below job description and let me know your interest. Job Role : Expert Skills- Computer System Validation Validating ERP to AWS Data migration process Validating Data migration project JD- Experience in the Pharmaceutical, biotechnology, or medical device industry 5+ years experience with System Development Lifecyle 5+ years experience in Computer System Validation (Based on the role selected) Experience in FDA and or Global regulated environment with good understanding of GxP standards and Risk based validation. 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 Hiring for CSV Validation Lead - Raritan, NJ (Hybrid) [email protected] |
| [email protected] View all |
| Sat Aug 24 00:48:00 UTC 2024 |