New

QA Technician

DiaSorin
United States, Texas, Austin
Jun 29, 2026
Obsessed by Science. Entrepreneurial by Nature. United by Purpose. Diasorin is a global leader in immunodiagnostic and molecular diagnostic solutions, advancing science to improve patient outcomes worldwide. For more than 50 years, we have combined scientific rigor with an entrepreneurial mindset, operating with a strong commitment to innovation, accountability, and results to deliver trusted diagnostic solutions. As the Diagnostics Specialist, Diasorin continuously invests in research, technology, and people. Guided by our values of operational excellence, customer focus, and teamwork, we empower teams to think boldly, act decisively, and transform ideas into meaningful impact across one of the industry's broadest specialty diagnostic portfolios. When you join Diasorin, you are not just filling a role. You are helping build what comes next. Why Join Diasorin Build What Matters Take ownership, challenge the status quo, and contribute directly to solutions that improve patient care worldwide. Innovate with Agility at a Global Scale Work in an entrepreneurial environment that enables speed, collaboration, and global impact. Grow in a People-Centered Culture Thrive in a culture that values accountability, inclusion, and continuous development. Job Scope The Quality Assurance Technician I is responsible for reviewing and verifying Device History Records (DHRs) toensure compliance with internal procedures, FDA regulations (21 CFR Part 820), and ISO standards (e.g., ISO13485). This role supports the release of intermediate materials and finished medical devices and ensuresproduct quality and regulatory compliance. Key Duties and Responsibilities Review completed Device History Records (DHRs) and other quality records for completeness, accuracy, and compliance with documented procedures and execute product release under a production schedule Verify that all required production, inspection, and test documentation is complete and meets release criteria Identify and document any discrepancies or non-conformances found during DHR review, generating Non-Conformance Reports (NCs) as needed Log, file, maintain and archive various QA reports & records Maintain and track key performance metrics Perform QA Gemba walkthroughs of manufacturing operations to drive continuous improvement and compliance Assist in continuous improvement of DHR review processes and related quality procedures Participate in quality investigations (e.g., CAPA, NCs) related to DHR errors or product quality issues as needed Assist other Quality Assurance personnel in data collection as needed Other duties as assigned Education, Experience, and Qualifications Associate's Degree Associate degree in a life science or engineering or equivalent related experience Preferred Or H.S. Diploma Required Minimum Years of Experience 1+ Years Experience in FDA regulated manufacturing environment, previous Quality experience Preferred 1+ Years Experience with participating in formal audits preferred Preferred Certification in a quality discipline preferred, such as CQT, CCT, CQI, etc. Preferred Training and Skills Good verbal and written communication skills Computer skills (Microsoft Windows and Office programs), familiarity with Oracle preferred Highly organized with proven time management and prioritization skills Ability to handle the pressure of meeting tight deadlines What we offer Diasorin offers a competitive rewards package focused on your overall well-being. We are proud to offer a comprehensive plan of health benefits, retirement and financial well-being, time off programs, well-being support and perks. Benefits may vary by role, country, region, union status, and other employment status factors. You may also be eligible to participate in an annual incentive program. An incentive award, if any, depends on various factors, including, individual and organizational performance. Diasorin is committed to building a workplace where people feel empowered to contribute ideas, take ownership, and grow their careers. We believe diverse perspectives strengthen innovation and help us deliver meaningful impact for patients and customers worldwide. Diasorin is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by applicable law. This posting and recruitment process are subject to applicable local laws and regulations in the country where the position is located. Additional employment disclosures, candidate rights, and employment conditions may apply based on local jurisdiction. Individuals hired will be required to verify identity and eligibility to work and may be subject to a background check and drug screening where permitted by law. Diasorin is committed to providing reasonable accommodations for qualified individuals with disabilities during the application process. If assistance is required, please contact hr@diasorin.com. Recruitment Fraud Notice Diasorin never requests payment, financial information, or personal banking details from candidates at any stage of the recruitment process. Official communications from Diasorin recruiters will only come from a verified @diasorin.com email address. If you have questions about the legitimacy of a recruitment communication, please contact hr@diasorin.com for verification. Unauthorized third-party recruiting agencies may not submit candidates for this position without prior written authorization from the Diasorin Human Resources Department.