The Sr. Medical Underwriting Nurse Manager is responsible for leading clinical risk strategy and underwriting excellence within the Small Group market, reporting to the VP of Small Group Underwriting. This role combines advanced clinical expertise with underwriting leadership to drive profitable risk selection, guide pricing strategy, and support renewal and new business growth. Contributes to the development of underwriting guidelines for clinical underwriting risk management Guides underwriting strategy in collaboration with VP of Small Group Underwriting and internal stakeholders for targeted profitable risk selection Provides expert clinical consulting on underwriting risk initiatives in collaboration with Actuarial Partners, Sales, IT, Underwriters, and Compliance Manages direct reports and relationships with key stakeholders as delegated with mentorship and clinical consultations as needed Helps formulate and execute strategy of how to hit or exceed key target metrics such as loss ratio, underwriting expense, close ratio, and underwriting turnaround times Develops and manages relationships with internal business partners, including actuarial, sales, IT, and compliance Responsible for a book of business of renewing accounts and writing new business at profitable levels Uses various systems, tools, and resources to obtain necessary data and accurately complete and track assigned work Evaluates the eligibility of groups and the participating employees at the time of a new business quote Calculates rates, evaluates different financial arrangements, interprets pricing policy, and adapts to unusual situations Identifies questionable claim patterns of renewal clients and evaluates competitors’ claims experience for prospective clients Applies corporate risk management policies and adjusts for unusual situations Enforces Optimyl's business rules (participation, product availability, etc.) Analyzes individual member risk and aggregates to the total group Supports other internal initiatives including underwriting policies and procedures, training, fraud detection, corporate compliance, and product development efforts Completes renewals, prospective quotes, and review of lower-level analyst work in accordance with production and timeliness standards Adapts to changing priorities as quotes come in from different markets Communicates recommendations of policy adaptation to accommodate client-specific situations Serves as a clinical SME to sales and account management Guides, assists, and provides technical assistance to lower-level analysts

The Principal Design Quality Engineer will be expected to contribute to maintaining the safety and efficacy of Cleerly’s software medical device products. You will be a key member of the product development team, ensuring that our software medical devices are developed in compliance with our ISO 13485 certified Quality Management System and applicable standards and regulations. Act as the design quality engineering lead on software development project teams, providing guidance and oversight to ensure compliance with the Quality Management System (QMS) and external regulations. Review and approve design and development documentation, including user needs, requirements specifications, software architecture, and verification & validation (V&V) plans, protocols, and reports. Ensure all design control activities are compliant with ISO 13485, IEC 62304, and FDA 21 CFR Part 820. Facilitate, document, and maintain risk management activities according to ISO 14971 throughout the product lifecycle, from initial concept through post-market surveillance. Collaborate with engineering teams to ensure test methodologies are robust, effective, and well-documented for verifying and validating the software medical device. Maintain the Design History File (DHF) for assigned projects, ensuring they are complete, accurate, and ready for audits and regulatory inspections. Provide quality oversight for the software development lifecycle (SDLC) within an agile development environment, ensuring quality is built into the process. Participate in design reviews, technical reviews, and other project meetings to ensure quality considerations are addressed and integrated. Participate in software issue triage to determine risk of issues to the medical device and aid in development prioritization. Support the investigation of design-related complaints and contribute to Corrective and Preventive Action (CAPA) activities as required. Team leader who, in conjunction with management, designs and drives team-wide and company-wide training in the above areas.

• Ensure structured, accessible technical documentation • Act as a liaison between Product, Development, QA, and Operations • Create and maintain the technical knowledge base

• At Omie, quality is built from the first requirement. • We are looking for someone who will grow within a dynamic team and work to ensure not only product excellence but also an outstanding user experience — supported by consistent, reliable, and usage-oriented documentation. • We value people who pay attention to details with critical thinking and who see quality as a strategic part of the entire software and documentation lifecycle. • Manual Testing: Perform manual testing on web (across different browsers), mobile, and API environments, validating features, flows, and user experience. • Test Automation: Develop and execute automated tests to increase efficiency, coverage, and reliability in validation cycles. • Bug Management: Report bugs in a structured and clear manner, following the full cycle from issue report through fix and final delivery validation. • Product Documentation: Create and maintain functional and user-facing documentation with a focus on clarity and usability. • Technical Documentation: Produce and update internal documentation describing product behavior, new features, and relevant technical decisions. • Cross-functional Communication: Participate in project follow-up meetings with stakeholders, helping to align quality, product, and engineering teams. • Proactivity: Collaborate proactively with development, product, and support teams, always focused on delivering value and continuously improving the user experience. • Technical Stack: Work with collaboration and versioning tools such as Coda (for documentation and tests), GitHub (for issue tracking), and Postman (for API testing and validation).