Nevro (NYSE: NVRO) is a global medical device company headquartered in Redwood City, California. We are focused on delivering comprehensive, life-changing solutions that continue to set the standard for enduring patient outcomes in chronic pain treatment. The company started with a simple mission to help more patients suffering from debilitating pain and developed its proprietary 10 kHz Therapy, an evidence-based, non-pharmacologic innovation that has impacted the lives of more than 100,000 patients globally.
Nevro’s comprehensive HFX™ spinal cord stimulation (SCS) platform includes a Senza SCS system and support services for the treatment of chronic trunk and limb pain and painful diabetic neuropathy. Senza®, Senza II®, Senza Omnia™, and Senza HFX iQ™ are the only SCS systems that deliver Nevro's proprietary 10 kHz Therapy. HFX iQ, Nevro’s latest innovation, is the first and only SCS System that uses Artificial Intelligence to optimize and maintain pain relief using each patient's response1.Nevro’s unique support services provide every patient with an HFX Coach™ throughout their pain relief journey and every physician with HFX Cloud™ insights for enhanced patient and practice management.
Nevro also recently added a minimally invasive treatment option for patients suffering from chronic sacroiliac joint ("SI joint") pain and now provides the most comprehensive portfolio of products in the SI joint fusion space, designed to meet the preferences of physicians and varying patient needs in order to improve outcomes and quality of life for patients.
Job Summary & ResponsibilitiesIT 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.
Role RequirementsBachelor'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
Skills and Knowledge
Target Pay Range
$154,116-170,000/year
EEO StatementNevro offers equal employment opportunity, regardless of race, color, creed, religion, national origin, marital or family status, sex, sexual orientation, gender expression (including religious dress and grooming practices), gender (including pregnancy, childbirth or medical condition related to pregnancy or childbirth), physical or mental condition, protected veteran status, disability, age or other characteristics protected by laws.
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