Sr. RA Specialist

Who We Are

Noah Medical is building the future of medical robotics. Our next generation robotic platform targets early diagnosis and treatment of patients across multiple indications. We are looking for exceptional engineers and key team members. Our incredibly talented team of engineers innovators and industry leaders bring years of experience from the top healthcare companies in the world including Intuitive Auris Stryker Johnson & Johnson Boston Scientific Verb Surgical Mako Think Surgical Medrobotics and Hansen. We are looking for talented motivated and ambitious team members to revolutionize robotic surgery. 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! A Day In The Life Of Our Sr. RA Specialist Regulatory Strategy & Product Development Support development and execution of global regulatory strategies for new and existing medical devices. Provide regulatory guidance to cross-functional teams throughout product development design changes and sustaining engineering activities. Assess regulatory impact of product process labeling software and manufacturing changes. Participate in design reviews and product development activities to ensure regulatory requirements are incorporated. Regulatory Submissions & Registrations Prepare and submit regulatory submissions including FDA 510(k)s international registrations technical documentation and other regulatory filings as required. Support compilation and maintenance of Design and Development Files (DDF) Technical Documentation and regulatory submission dossiers. Coordinate submission activities with regulatory agencies notified bodies and international regulatory authorities. Track submission status and ensure timely responses to regulatory inquiries. Regulatory Compliance Monitor and interpret evolving regulatory requirements and standards including FDA EU MDR ISO 13485 MDSAP and other applicable regulations. Ensure ongoing compliance with global regulatory requirements throughout the product lifecycle. Support implementation of new regulatory requirements within the Quality Management System (QMS). Maintain product registrations licenses and regulatory approvals. Labeling & Promotional Review Review product labeling Instructions for Use (IFUs) marketing materials and promotional content for regulatory compliance. Ensure claims are adequately supported and consistent with approved regulatory submissions. Audits & Inspections Support internal audits external audits notified body assessments and regulatory inspections. Provide regulatory subject matter expertise during audits and inspections. Assist in developing responses to audit findings and regulatory observations. Cross-Functional Collaboration Collaborate with Quality Product Development and Manufacturing teams to support regulatory objectives. Support complaint investigations CAPAs post-market surveillance and field actions from a regulatory perspective. Participate in management reviews and regulatory compliance reporting activities. Regulatory Intelligence Monitor industry trends regulatory changes guidance documents and standards updates. Communicate regulatory changes and assess business impact. Recommend actions to maintain compliance and support business objectives.

About You

Bachelor's degree in Engineering Life Sciences Biomedical Engineering Regulatory Affairs or a related technical discipline. Advanced degree preferred. 5+ years of Regulatory Affairs experience within the medical device industry. Experience preparing and supporting FDA 510(k) submissions. Experience supporting international registrations and regulatory submissions preferred. Working knowledge of medical device development processes and design controls. Experience with Class II and/or Class III medical devices preferred Strong knowledge of FDA 21 CFR Part 820 and applicable FDA regulations EU MDR (2017/745) ISO 13485 ISO 14971 Risk Management MDSAP requirements Medical device labeling requirements Regulatory Affairs Certification (RAC) preferred. Experience with software-enabled medical devices and cybersecurity submissions preferred. Experience supporting global markets including EU Canada Australia and Asia-Pacific regions. Experience interacting directly with FDA notified bodies and international regulatory agencies Strong project management and organizational skills. Excellent written and verbal communication skills. Strong analytical and problem-solving abilities. Ability to work independently with minimal supervision. Proficiency with Microsoft Office and electronic Quality Management Systems (eQMS) LI-Hybrid Pay Transparency The

Pay Range

for this position is listed. Noah Medical offers a comprehensive benefits package including competitive pay health insurance 401K and stock purchase plans tuition reimbursement paid time off plus holidays and a flexible approach to work with remote hybrid field or office work schedules. Actual pay will be adjusted based on an individual's skills experience education and other job-related factors such as location as permitted by law. Total compensation may also include additional forms of incentives. California

Pay Range

$109000 $136000 USD

Benefits

& Perks (For Full Time Employees) Competitive Salary Comprehensive health insurance including Medical Dental and Vision + HSA and FSA options Equity & Bonus Program Life Insurance (company paid & supplemental) and Disability insurance Mental health support through medical insurance programs Legal and Pet Insurance 12+ paid holidays Flexible Time Off + Sick Time Paid parental leave In-office snacks and beverages In-office lunch stipend Learning & Development Opportunities On-demand online training and book reimbursement Team building and company organized social and celebration events Noah Medical may offer remote hybrid or onsite work arrangements within the state of California depending on the specific team and/or role where applicable. Noah Medical is an Equal Opportunity Employer. We celebrate diversity and are committed to ensuring an inclusive environment for our employees. Applicants are considered for all positions without regard to race color religion sex or gender gender identity or expression sexual orientation national origin ancestry age genetic information physical or mental disability marital or protected military or veteran status or any other consideration made unlawful by federal state or local laws. Please visit our Careers Page to view our latest openings. NO AGENCIES PLEASE Please do not outreach to any managers or submit any resumes without a signed agreement from Talent Acquisition. Resumes shared with anyone at Noah Medical without a signed agreement will be considered your gift to us and no fee will be paid