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Net2Source (N2S) • Princeton, New Jersey, United States
Salary: 21 CFR Pa
Role & seniority: Senior/Lead Computer System Validation (CSV) compliance specialist for regulated environments (6+ years experience)
Stack/tools: MS Office (advanced), Visio; electronic document management systems (Documentum, Qumas, SharePoint); application lifecycle tools (Client ALM, JIRA); ITSM systems (ServiceNow, SAP Solution Manager)
Lead/facilitate CSV risk assessments and identify governing regulations and validation deliverables
Review and approve validation deliverables and change requests; monitor project validation status
Train/guide stakeholders on quality, documentation and validation practices; ensure regulatory compliance and communication across teams
In-depth knowledge of FDA, MHRA and global health authority regulations; 21 CFR Part 11 validation scope
Expertise in Good Documentation Practices and Good Testing Practices
Ability to create and review CSV documentation (Requirements/Design specs, CSV Risk Assessments, Test Plans/Reports, Data Migration, Traceability Matrix, Release to Production)
Independent, self-directed work style in a highly matrixed organization; strong written and oral English communication
Experience with training business users; background with ALM, ELM, or lifecycle management tooling; familiarity with project document standards
Location & work type: Not specified; no location or explicit vacation/remote details provided
Job Description: 6+ years experience Apply FDA, MHRA, and other applicable global health authority regulations to the development of computer systems supporting regulated business processes Follow SOPs and industry best practices Possess Expertise on Good Documentation and Good Testing Practices, in order to train those within the business that are less familiar. Facilitate the Computer system Validation Risk Assessment to identify governing regulations and validation deliverables during the development of the computer system Review validation deliverables for projects which are contracted to third party suppliers Maintain close communication with stakeholders and team members to keep apprised of computerized system needs, impacts on computer validation, project validation status, and other relevant issues Assist in planning, implementing, and documenting user acceptance testing
Direct and review testing Provide guidance on quality issues that affect the integrity of the data or the system Obtain and respond to QA review Participate in establishing standard quality and validation practices Independently assess compliance practices and recommend corrective actions Approve validated computer system related change requests Monitor regulatory and inspection trends and advise the business on suitable action Ability to create documents to an existing document standard. Able to develop all documentation required for a 21 CFR Part 11 validated project, including Validation Plans and Summaries.
Advanced knowledge of complete MS Office suite and Visio. Firm understanding of technology platforms as needed for project. Experience with electronic document management systems (e.g. documentum, Qumas, SharePoint etc.); application development and lifecycle management (e.g. Client ALM, JIRA, etc.); and IT service management systems (e.g. ServiceNow, SAP Solution Manager, etc) Excellent oral and written communication skills in English. Strong expertise and ability to interview and accurately interpret communication requirements of team members. Once trained, have the ability to work independently on CSV projects with minimal oversight. Ability to perform in a highly matrixed organization structure