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 & ResponsibilitiesThe Production Supervisor position will directly be responsible for the production and line personnel and support the implementation of the site strategy for manufacturing to ensure the manufacture of high-quality products and to facilitate compliance with regulatory requirements.
ESSENTIAL DUTIES & RESPONSIBILITIES:
The duties and responsibilities for this position include, but are not limited to, the following:
Oversee operations efficiency and standardization in the production lines.Directly responsible for the production and quality of the product, as well as line personnel.Analyze and evaluate process improvements in order to reduce defects and scrap and/or improve yields.Follow procedures established for each operation, and keep work areas organized and clean at all times.Participate and/or lead problem-solving processes, whether due to increasing trends on complaints, defects, scrap, or low productivity, among others.Monitors compliance within company policies and procedures (e.g., compliance with FDA, ISO 13485, or other regulations).Comply with all safety and health regulations for the position and the direct reports.Comply with all quality regulations for the position and the direct reports.Responsible for ensuring that production processes are aligned with the company's energy policy commitments. Will support improvement analysis processes that impact production processes, enhancing quality and optimizing energy consumption.Ensure compliance of the organization's management systems to guarantee effectiveness and adherence to established policies, standards, and regulatory requirements.
Role Requirements Bachelor’s degree or an equivalent combination of education and work experience 3 -5+ years of experience minimum experience in the medical industry. 3 Years experience in a supervisory capacityExperience analyzing and presenting detailed or advanced metrics using tools Experience in internal and external audits regarding the Quality Management SystemDemonstrated proficiency in manufacturing systems used to collect data and control/monitor processes. Demonstrated capacity to effectively lead/influence peers and other functions towards organizational goalsDesirable at least one certification-related or applicable to the medical industry. For example, CQE, 6Sigma Green Belt and/or Black Belt, lean coach, problem-solving techniques, etc. Skills and Knowledge Flexible attitude and the ability to deal with changing assignments and prioritiesMust be self-motivated and capable of working under tight deadlinesAbility to work as a team member, as well as independentlyAbility to adapt well to fast-paced environments with changing circumstances, direction, and strategyExcellent communication and interpersonal skills; both written and verbalResults and detail-orientedAbility to plan and manage time effectivelyStrong teamworkDemonstrated knowledge of ISO and quality systems as FDA and OSHA requirements, as a plus Intermediate level of English
Target Pay Range
The final starting salary offer to the successful candidate will be determined by evaluating several factors, such as education, experience, knowledge, skills, internal equity, alignment with market data, and geography. *Nevro is a multi-state employer, so the target pay range may increase or decrease depending on the city/state.
Full-time Nevro team members enjoy a full suite of additional benefits such as market-leading medical, dental, and vision benefits, 401k matching, ample vacation time, pre-tax savings perks, tuition reimbursement, Employee Stock Purchase Plan (ESPP), short and/or long-term incentive opportunities, recognition awards, volunteer time off, and several employee resource groups that focus on supporting our Wellness, Leadership Development, and Diversity and Inclusion.
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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