Job Abstract

ID

2024-4512

Category

Clinical & Regulatory

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. 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.

Regulatory Affairs Manager, Redwood City, CA - Develop global regulatory strategies and submission activities for various new development and product modification of Nevro’s Senza spinal cord stimulation (SCS) system, an Implantable Class 3 medical device; ensure compliance with medical device regulations of U.S. federal code, FDA, E.U., and Australia; coordinate product development, commercialization, and post-launch product success and supports the marketplace competitiveness; develop clinical trial plans and reports which support clinical indication expansion products, in collaboration with cross-functional teams; prepare IDE, 510(k), PMA, CE Mark submissions; collaborate with R&D and Quality to determine and execute pre-clinical test plans in support of new product development regulatory submissions; apply regulatory knowledge in managing multiple projects; establish and lead communications with FDA, Notified Bodies, and other regulatory agencies; provide leadership and regulatory guidance to ensure timely and accurate documentation for regulatory submissions; apply scientific background to develop trial plans and reports; maintain knowledge of competitive technologies to stay current; develop, document and implement regulatory strategies for new technologies and product modifications. Remote work from anywhere in the US is permitted. (No agencies or phone calls please.) #LI-DNI

Requires Master’s degree in Regulatory Affairs, Biomedical Engineering, or Medical Device Engineering, and six years of experience as a Regulatory Affairs Manager or Regulatory Affairs Specialist or related occupation in regulatory affairs, or a Bachelor’s degree in Regulatory Affairs, Biomedical Engineering, or Medical Device Engineering, and eight years of experience as a Regulatory Affairs Manager or Regulatory Affairs Specialist or related occupation in regulatory affairs.

Must possess Six years of experience with implantable Class 3 medical devices in the following:

• Developing clinical trial plans and reports which support clinical indication expansion products, in collaboration with cross-functional teams;
• Collaborating with cross-functional teams
• Determining and executing pre-clinical test plans in support of new product development regulatory submissions in collaboration with R&D and Quality;
• Providing leadership and guidance to ensure timely and accurate documentation for regulatory submissions;
• Preparing PMA submissions for the FDA and global regulatory submissions in the European Union and Australia

Remote work from anywhere in the US is permitted.

• Be viewed as a leader by your manager, peers, and subordinates.
• Be a problem solver and not just a problem communicator.
• Demonstrated experience in preparing 510(k) and PMA submissions for FDA.
• Demonstrated experience with global submissions (EU, Australia, Japan, etc.)
• Strong interpersonal and analytical skills.
• Excellent written and oral communication skills.
• Excellent organizational and multi-project management skills and attention to detail.
• Regulatory Affairs Certification (RAC) is preferred.

$126,938 to $155,000

Nevro 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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