| Technical Lead (CSV, Clinical Systems)-Raleigh, NC***Day 1 Onsite***Immediate Interview-HCL at Raleigh, North Carolina, USA |
| Email: [email protected] |
| From: Danish Azeez, Inherent technologies [email protected] Reply to: [email protected] Position: Technical Lead (CSV, Clinical Systems) Location: Memphis***Day 1 Onsite*** Duration: 1 Years Phone & Skype Client: HCL local only********************* Immediate Interview *ITAP Reference number BR Number Candidates Details Full Name (First ,Middle, Last) Current Location (City & State) Relocation Authorization (H-1,GC,US Citizen, TN,OPT) Primary Phone Number Email ID SSN (Last 4 digit) DOB (MM/DD) Total IT Experience Total US Experience Vendor Name Salary / Hourly Rate Skill Rating Mandatory Skills Hands on experience in Years Last used -Year Self-Rating (Scale 1-10) 1. 2. 3. 4. CSV, Computer System Validation, Clinical Systems Keywords : CSV, Computer System Validation, Clinical Systems, Safety Systems, Infrastructure Qualification, 21 CFR part 11, GAMP 5, ICH, EMEA, MHRA regulations Roles and Responsibilities Must Have 10 + years Experience in Validating GxP applications Experience in FDA and/or Global regulated environment with good understanding of GCP , GLP and Risk based validation strategy Provides consultation and counseling on Risk and Compliance module implementation in reference to regulatory quality Support Risk assessment Document Regulatory Requirements and Review Specification documentation (viz. User Stories, URS, FRS) Review and final Approval of requirements, Technical Design and Solution Architecture Plan, IQ, OQ and PQ pre and post execution documents Lead, Write, Review/ Approve Discrepancy Logs (final dispositions) Lead, Write, Review / Approve Requirement Traceability Matrix (RTM) and Validation Summary Reports Good to Have (secondary skills) Experience in Clinical systems like CTMS, CDMS, EDC, Veeva Vault, QMS and Safety Systems and Infrastructure Qualification Conduct Periodic Reviews of GxP Apps as per the frequency stated in the governing SOP and write Periodic review reports and Review and Approve Periodic Review Reports Tracks the Periodic review findings and open CAPA s to a closure Review and Approve System Support and Operations plan Participate in and support Audits. Contribute and Review/ Approve Decommissioning Plans & Decommissioning Reports Contribute, Review/ Approve deliverables for Change Management Support Maintain validation documentation throughout product lifecycle viz.as a result of Change, Periodic Review, Audits Communication Immaculate communication and handles multiple clients/ projects Works in Consulting capacity (1.) To ensure process improvement and compliance, and participate in technical design discussion and to review technical documents (2.) Co-ordination with On-Site Engineers and attending customer calls (3.) Raising risks, issues and escalation to senior management and customer (4.) To create all quality documents, collect metrics data and conducting Audits. To perform Value creation and KM activities. (5.) To create project plans and keep track of schedule for on time delivery as per the defined quality standards Keywords: materials management information technology green card trade national Colorado Idaho Tennessee |
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| Fri Jan 19 19:44:00 UTC 2024 |