Company:
Katalyst Healthcares & Life Sciences
Location: Raleigh
Closing Date: 17/06/2024
Hours: Full Time
Type: Permanent
Job Requirements / Description
Responsibilities:
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.
Requirements:
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 a result of Change, Periodic Review, Audits.
Immaculate communication and handles multiple clients/ projects
Works in Consulting capacity.
To ensure process improvement and compliance, and participate in technical design discussion and to review technical documents.
Co-ordination with On-Site Engineers and attending customer calls.
Raising risks, issues and escalation to senior management and customer.
To create all quality documents, collect metrics data and conducting Audits. To perform Value creation and KM activities.
To create project plans and keep track of schedule for on time delivery as per the defined quality standards.
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.
Requirements:
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 a result of Change, Periodic Review, Audits.
Immaculate communication and handles multiple clients/ projects
Works in Consulting capacity.
To ensure process improvement and compliance, and participate in technical design discussion and to review technical documents.
Co-ordination with On-Site Engineers and attending customer calls.
Raising risks, issues and escalation to senior management and customer.
To create all quality documents, collect metrics data and conducting Audits. To perform Value creation and KM activities.
To create project plans and keep track of schedule for on time delivery as per the defined quality standards.
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