Posted in Other about 6 hours ago.
IT Compliance/Validation Manager for Nevro Corp, Redwood City, CA.
Responsible for all aspects of IT compliance, testing, and system/software changes. Manage IT’s Computer System Validation (CSV) Programs and Risk, and Compliance management of IT operations that address Internal Control over Sarbanes-Oxley. Apply knowledge and experience in GxP, CSV, SOX, ITGC, 21 CFR Part 11, and ITIL frameworks related to IT delivery services. Perform Software Development Life Cycle (SDLC) or relevant framework. Coordinate internal/external coordination audit resources with IT, while also managing Nevro’s Change Management Process (CMP) and Change Advisory Board. (CAB). Develop testing strategy across IT applications for GxP and non GxP applications. Coordinate with appropriate groups (executive management, internal audit, external audit, etc.) regarding regulatory changes and industry standards and manage a team including direct reports and consultants. Maintain IT’s Computer Validation System (CVS) SOP and lead validation efforts related to new and existing applications by working in partnership with key company stakeholders including Quality, Validation, Legal, Finance, and HR. Apply understanding of computer system development process and FDA regulations to perform validation activities throughout validation life cycle, including developing documentation evidence, managing/executing protocols, initiating change procedures, and ensuring quality. Perform IT quality and compliance in an FDA-regulated environment (GxP). Design and execute validation strategy for implementation of new systems. Conduct IT delivery services, process improvements, and assessment of IT control environment. Understand company software systems to navigate system to analyze test results. Manage/coordinate validation project activities through project phases. Develop validation documents like plan and summary reports in alignment with internal procedures. Oversee internal and external team members to execute validation activities. Assess upcoming projects. Support manufacturing systems validation, including MES and ERP. Define and manage validation activities based on project. Allocate tasks to internal and external team members. Ensure generation of required validation deliverables like Validation plan, Test protocols, Test summary reports, Validation summary reports, etc. based on projects. Define timelines validation/ test activities and define project timelines in collaboration with project management team. Track and ensure completion of validation tasks by coordinating with team members. Optimize resource utilization. Train validation resources on process and procedures. Manage direct employees and consultants. Remote work permitted within normal commuting distance at employer’s discretion.
Bachelor's degree in Computer Science, Regulatory Affairs, Validation Engineering, or related field and 5 years of progressive post baccalaureate experience as a validation engineer or regulatory specialist.
Must possess 5 years of experience with:
- Software Development Life Cycle (SDLC) or relevant framework
- Performing IT quality and compliance in an FDA-regulated environment (GxP)
- Working with CSV, 21 CFR Part 11, and ITIL frameworks as related to IT delivery services
- IT delivery services, process improvements, and assessment of IT control environment
- Development and review of IT and Quality SOP’s
-Strategic planning validation activities for projects related to IT applications
PI256861849
SCIEX |
Integrated DNA Technologies (IDT) |
Haven Behavioral Healthcare |
Haven Behavioral Healthcare |
Haven Behavioral Healthcare |