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 & ResponsibilitiesThis is a full-time temporary position with a 3-4 month duration.
The Quality Engineer is responsible for activities including but not limited to supporting sustaining processes and supplier nonconformances. This is a hands-on role where the Quality Engineer will apply knowledge of engineering, risk management, supplier management, and quality principles/practices towards the production of implantable medical devices. This position will report to the Principal Quality Engineer onsite at the Nevro-Vyrsa facility in King of Prussia, PA.
Role Requirements 2 to 3 years of hands-on Quality experience in the medical device industry with direct experience investigating and resolving nonconformances of FDA Class-I & Class-II medical devices; preferably on orthopedic implants and instruments. Bachelor's degree in engineering or technology (mechanical or biomedical preferred). Equivalent years of experience may be substituted for the education requirement.Perform other duties as assigned. Skills and Knowledge Working knowledge of Root Cause Analysis, Corrective Action & Prevention methodologies for systemic nonconformity investigation and mitigations.Strong problem-solving skills.Read and understand engineering drawings inclusive of Geometric Dimensioning & Tolerancing (GD&T)Demonstrated ability to manage multiple priorities in a fast-paced environment. 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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