- If you're passionate about CSV and SDLC concepts like V-Model, Waterfall, and Agile Scrum, we want to hear from you.
- But wait, there's more We need someone who's not just familiar with regulations and guidelines in the life sciences/pharma industry (think GAMP, GxP, 21 CFR Part 11, EU Annex 11, GDPR), but who lives and breathes them.
- And if you happen to have a secret weapon knowledge of Pharmacovigilance (PV) computer systems well, that's music to our ears.
- But here's the kicker: we need someone who's not just talk. We need someone who's handson, who's tackled validation deliverables like URS, FRS, Test Scripts, and Validation Summary reports with finesse.
- Act as SME for Computer System Validation (CSV) for GXP based computerized systems developed internally and deployed for customer implementations.
- Work closely with cross functional groups, including Design, Development and Business Analysts to deliver results.
- Define riskbased validation strategy & execute in line with company's QMS (Quality Management System)
- Participate in assessments including System impact assessment, functional risk assessment, data integrity assessments etc.
- Define test strategy, build test scenarios as necessary based on criticality of requirements,
- Testing effort estimation and resource management Manage test execution, Perform CAPA (Corrective and Preventive Actions) and RCA (Root Cause Analysis) for test incidents and deviations
- Review, and report Test Results in line with System Testing Life Cycle.
- Participate in endtoend change management including handling deviations both during the project and operation phase.
- Author and peer review of key validation documents, as per Good Documentation Practices.
- Validation Plan, Change Request Risk Assessment Report
- Test Scripts: IQ, OQ, PQ/UAT
- Test Incident Reports
- Trace Matrix
- Test/Validation Summary
- Good knowledge of CSV and SDLC concepts: V-Model, Waterfall, Agile Scrum etc.
- Exhibit good understanding of regulations/guidelines applicable to Life sciences/Pharma industry like GAMP, GxP, GDP, 21 CFR Part 11, EU Annex 11, GDPR etc.
- Knowledge of Pharmacovigilance (PV) computer systems (Preferred)
- Sound knowledge of validation of GxP systems (on cloud / on premise solutions)
- Hands on with Validation deliverables like URS, FRS,
- Risk Assessment, Configuration specifications,
- Validation Plan, IQ/OQ/PQ Test scripts (authoring/review/execution), Trace matrix & Validation Summary report.
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Validation Consultant - Noida, India - Neufvasi Digital Solutions Private Limited
Description
We're on the hunt for a validation virtuoso with experience of 7+ years to join our client at NoidaJob Description :