Noah Medical

This position provides hands-on technical guidance and leadership from a Quality perspective to the team throughout all stages of product development up to and including technology transfer and commercialization.. BS in Computer Science, Electrical Engineering, Biomedical Engineering, Mechanical Engineering, or other related programs.. Minimum of 8 years of Quality Engineering work experience in the medical device field with complex medical devices, i.e. devices that include capital hardware, disposable hardware, and software.. Comprehensive health insurance including Medical, Dental and Vision + HSA and FSA options. Learning & Development Opportunities: On-demand online training and book reimbursement

quality engineer

<div>About The Team:
Join our Quality team at Noah Medical, where you'll play a pivotal role in driving innovation and product leadership in medical robotics. We're a hands-on, technical, and solution-oriented, and accountable team, seeking like-minded individuals to join us. Utilizing a data-driven approach, we tackle challenges and fuel innovation. Committed to exceeding FDA and international regulatory standards, we take initiative, optimize processes, and implement agile quality management systems to foster continuous improvement. Our ultimate goal is to make a meaningful impact on patients' lives by setting new benchmarks and breaking barriers in the field of medical robotics. Come join us as we shape the future together!
This position provides hands-on technical guidance and leadership from a Quality perspective to the team throughout all stages of product development up to and including technology transfer and commercialization. We are looking for someone that is highly motivated and solution oriented; you must be a self-starter, team builder, and excellent communicator. This is a Full Time Salaried position.
A Day In The Life Of OurStaff DQA Software Engineer:
<ul>
<li>Provide hands-on guidance for establishing good product and system design requirements, design specifications, detailed designs, verification and validation activities, and planning documentation. </li>
<li>Understand clinical applications, workflow and user needs</li>
<li>Develop software related verification and validation strategy for the R&D organization and ensure the execution of the strategy.</li>
<li>Serves as a technical resource for risk management activities for software in compliance with ISO 14971 and IEC 62304.</li>
<li>Develop test plans, and test cases based upon the product and component level requirements.</li>
<li>Partner with Human Factors SMEs and R&D to assess the usability of the software throughout design and development</li>
<li>Review and approve V&V system maintenance such as reworks and modification and tracking related to software upgrades.</li>
<li>Perform root cause analysis of identified design issues and identify appropriate corrective and preventive action. Use the NC and CAPA systems as needed to structure activities.</li>
<li>Perform audits of Design History Files and support both internal and external audits.</li>
<li>Support Regulatory Affairs with relevant submissions, approvals, requests, and inquiries.</li>
<li>Partner with PMO to apply project management tools in order to define project deliverables and establish a project schedule.</li>
<li>Work collaboratively and efficiently in a fast-paced environment with minimal supervision and guidance.</li>
<li>Maintain trained status for, and comply with all relevant aspects of Noah Medical Quality Management System to ensure product and support regulatory compliance. </li>
<li>As the voice of quality, this role will apply and promote best-practice use of statistical tools and techniques throughout the organization.</li>
<li>Other QMS activities not specified here and as assigned.</li>
</ul>
About You:
<ul>
<li>BS in Computer Science, Electrical Engineering, Biomedical Engineering, Mechanical Engineering, or other related programs.</li>
<li>Minimum of 8 years of Quality Engineering work experience in the medical device field with complex medical devices, i.e. devices that include capital hardware, disposable hardware, and software. and a minimum of 3 years’ experience in a development QE function.</li>
<li>Experience in meeting Design Control and DHF requirements with NPD teams.</li>
<li>Well versed in the complete Quality Management System to meet US FDA and ISO/MDR requirements with an emphasis on IEC 62304.</li>
<li>Experience with Risk Management, FMEA, Hazard Analysis.</li>
<li>Experienced with statistical skills to define/train on test sample size and data analysis techniques.</li>
<li>Experienced in Microsoft Office, Google Suite, JIRA, Jama, and ePLM/eQMS systems.</li>
<li>Must be a self-starter, team builder, and excellent in verbal and written communication.</li>
<li>Preferred: Certifications: CQE, CQA(BM), CQM, 6 Sigma, etc.</li>
<li>Passionate about SW and technologies for healthcare</li>
</ul>
Workplace Type: Hybrid
Benefits & Perks (For Full Time Employees):
<ul>
<li>Competitive Salary</li>
<li>Comprehensive health insurance including Medical, Dental and Vision + HSA and FSA options</li>
<li>Equity & Bonus Program</li>
<li>Life Insurance (company paid & supplemental) and Disability insurance</li>
<li>Mental health support through medical insurance programs</li>
<li>Legal and Pet Insurance</li>
<li>12+ paid holidays, 15-20 days of PTO + use-what-you-need sick days</li>
<li>Paid parental leave</li>
<li>In-office snacks and beverages</li>
<li>In-office lunch stipend</li>
<li>Learning & Development Opportunities: On-demand online training and book reimbursement</li>
<li>Team building and company organized social and celebration events</li>
</ul></div>
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