Role Description The Senior Quality Control (QC) Engineer at Lamdax plays a vital role in ensuring the quality and reliability of our software products and solutions. You will lead quality assurance initiatives, design and implement testing strategies, and work closely with development teams to detect, prevent, and resolve defects. This role requires a detail-oriented professional dedicated to maintaining high standards and improving processes to deliver exceptional software products. - Develop, execute, and maintain comprehensive test plans, test cases, and automated test scripts to ensure software quality. - Conduct manual and automated testing for web, mobile, and backend applications. - Identify, record, and track defects, working closely with development teams to resolve issues. - Implement and enhance testing frameworks and tools to improve test coverage and efficiency. - Collaborate with cross-functional teams to understand requirements and define quality standards. - Analyze test results, provide thorough documentation, and report on product quality metrics. - Mentor junior QA engineers and contribute to team knowledge sharing and process improvements. Qualifications - 5+ years of experience in software quality control or assurance, preferably in Agile environments. - Strong knowledge of QA methodologies, tools, and processes. - Proficiency in automated testing tools and scripting languages such as Selenium, JUnit, TestNG, or similar. - Experience with performance, functional, regression, and integration testing. - Familiarity with CI/CD pipelines and defect tracking systems like JIRA. - Excellent analytical, problem-solving, and communication skills. - Ability to work collaboratively in cross-functional teams and mentor junior members.

Role Description We are looking for a Quality Assurance Engineer to join Oura’s Medical Device team to help us ensure we are compliant with the applicable standards and regulations governing the development of medical device software at Oura. We call this role the Quality Assurance Champion. You will bridge the gap between rigorous regulatory compliance and the fast-paced innovation of our Software as a Medical Device (SaMD) development teams. - Develop, implement, and manage QMS processes to ensure compliance with international standards and internal requirements. - Support continuous improvement to the QMS by identifying areas for improvement and engaging in remediation. - Support the timely investigation of complaints, conduct thorough change impact assessments, and manage Corrective and Preventive Actions (CAPAs) to resolution. - Lead the functional configuration and optimization of the eQMS toolset, ensuring workflows are streamlined and the platform evolves to meet scaling business needs. - Develop and deliver training programs to empower Oura teams with a deep understanding of quality requirements and best practices. - Manage supplier control processes to ensure all partners consistently align with Oura’s rigorous quality benchmarks and compliance standards. - Collaborate with Oura’s SaMD feature development teams by providing technical and quality support during the development, testing and deployment of software. - Contribute in the compilation, review and approval of all technical documentation for SaMD development. - Support internal and external audits and inspections as a QMS subject matter expert. Qualifications - Degree in: Biomedical/Mechanical Engineering or related technical or scientific discipline. - 3+ years of experience working in a regulated environment, managing Quality Management Systems under ISO 13485:2016 and the MDSAP. - Working knowledge and application of device regulations (21 CFR 820 and EU MDR 2017/745). - Strong background in standards compliance (ISO 13485:2016, ISO 14971, IEC 62304, IEC 62366-1). - Familiarity with eQMS software tooling and experience in implementing, validating, and improving digital quality workflows. - Direct experience participating in regulatory inspections (e.g., FDA, Notified Body) and conducting or supporting internal/external quality audits. - Demonstrate ability to assess and provide technical guidance for software as a medical device (SaMD). - Demonstrate strong skills to organize, prioritize, and execute. - Must be detail oriented with strong leadership skills and excellent interpersonal, collaboration and communication skills. - You can sense and articulate why certain issues demand more diligence to ensure compliance to applicable regulations or standards. Benefits - Competitive Salary - Lunch benefit - Wellness benefit - Flexible working hours - Collaborative, smart teammates - An Oura ring of your own - Personal learning & development program - Wellness Time Off Company Description Oura is proud to be an equal opportunity workplace. We celebrate diversity and are committed to creating an inclusive environment for all employees. - Individuals seeking employment at Oura are considered without regard to age, ancestry, color, gender (including pregnancy, childbirth, or related medical conditions), gender identity or expression, genetic information, marital status, medical condition, mental or physical disability, national origin, protected family care or medical leave status, race, religion (including beliefs and practices or the absence thereof), sexual orientation, military or veteran status, or any other characteristic protected by federal, state, or local laws. - We will work to ensure individuals with disabilities are provided reasonable accommodation to participate in the interview process, to perform essential job functions, and to receive other benefits and privileges of employment.

Title: Senior Healthcare Industrial Engineer Location: Akron United States Job Description: Professional | Full Time Full-time, 40 hours/week Monday- Friday 8am-4:30pm Hybrid remote (2-3 days/week onsite) Summary: The Senior Healthcare Industrial Engineer serves as a key member of the hospital’s Management Engineering Program, playing a central role in establishing the function, setting analytical standards, and advancing operational efficiency across the organization. This individual will lead high‑impact projects that improve patient access, flow, standardization and resource utilization in a pediatric environment. The Senior Healthcare Industrial Engineer must be both highly strategic and hands‑on—capable of building infrastructure, developing methodologies, mentoring others across the organization, and delivering measurable outcomes. This role requires a systems‑thinker who is motivated by mission‑driven work that improves care for children and families. Responsibilities: - Lead complex, cross-functional performance improvement initiatives using systems engineering, industrial engineering, and operations research methods. - Apply advanced analytical tools (e.g., process mapping, simulation, optimization, statistical analysis, and human-centered design) to improve access, flow, quality, safety, and efficiency. - Partner with clinical, operational, and administrative leaders to identify priorities, frame problems, and co-develop solutions aligned with organizational strategy. - Translate complex analyses into clear, actionable recommendations for executive, clinical, and operational audiences. - Design and evaluate care delivery models, capacity management strategies, and operational workflows, with attention to pediatric and family-centered care. - Support implementation, change management, and sustainment of improvement initiatives, including measurement of outcomes and ongoing performance monitoring. - Serve as a trusted advisor to senior leaders on system design, tradeoffs, and data-driven decision-making. - Help establish standards, methodologies, and best practices for the Management Engineering program. - Contribute to the development and mentoring of future management engineering staff as the program grows. Other information: Technical Expertise - Proficiency in analytical and modeling tools (e.g., Python, R, SQL, Tableau, discrete event simulation platforms). - Strong understanding of continuous improvement methodologies. - Strong systems thinking and problem-solving skills. - Exceptional collaboration, facilitation, communication and relationship‑building skills Education and Experience - Education: Bachelor’s degree in Industrial Engineering, Systems Engineering, Operations Research, Management Engineering, or related field required. Master’s degree preferred. - Licensure: None - Certification: None - Years of relevant experience: At least 5 years of relevant experience. - Years of supervisory experience: None Full Time FTE: 1.000000 Status: Fixed Hybrid

Develop image processing algorithms and software for inspection systems, collaborate on data manipulation for production feedback, and transition prototypes into manufacturing-ready applications while supporting data analysis and documentation.