Quality Assurance Specialist jobs in Tel Aviv-Yafo

JOB DESCRIPTION: About Abbott Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology. Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You will have access to: • Career development with an international company where you can grow the career you dream of. • A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune. • A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists. The Opportunity This position is located in Tel Aviv within the Abbott Nutrition (AN) Division. We are seeking a highly motivated Quality Assurance Junior Specialist. The role is responsible for performing routine Quality Assurance tasks while also maintaining and continuously improving the implemented Quality Management System within the Israel affiliate. What You’ll Do: • Register and manage customer and HCP’s complaints in the Trackwise system, ensuring compliance with division timelines. • Oversee the Batch Release process for Abbott Nutrition products in line with global and local policies/regulations. • Review and manage invoice checks related to Batch Release activities. • Support Affiliate Training management in conjunction with the QA Supervisor/Manager. • Manage Document Control processes: initiate change requests, coordinate Subject Matter Expert (SME) edits, route documents for approval, and ensure timely completion and periodic reviews. • Review and evaluate Supplier Quality activities, including qualification, performance monitoring, audits, and SCAR (Supplier Corrective Action Request) closures, within required timelines. • Support inspection and audit readiness activities for the Affiliate, as directed by the QA Supervisor/Manager. • Assist in preparing Management Review presentations in collaboration with the QA Supervisor/Manager. • Monitor and support NCR (non-conformance) initiation, conduct root cause analysis, and oversee CAPA (corrective and preventative actions) implementation and effectiveness tracking. • Contribute to On-Market Events/Product Actions presentations in partnership with the QA Supervisor/Manager. Requirements: • Preferred: 2–3 years of experience in Quality Assurance or a related role. • Solid knowledge of Quality Systems and GxP standards. • Degree in Life Sciences or equivalent professional experience. • Self-motivated, driven and eager to learn. • Able to prioritize effectively and manage multiple tasks simultaneously. • Strong analytical and information-gathering skills. • Proactive and solution-oriented approach. • High level of accuracy and attention to detail. • Excellent communication skills (written and oral) in Hebrew and English. • Strong planning, prioritization and organizational abilities. • Effective interpersonal skills and ability to work collaboratively across teams and different stakeholders. • Proficiency in Microsoft Office applications, particularly Excel and Word Apply Now Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity. Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal. The base pay for this position is N/AIn specific locations, the pay range may vary from the range posted. JOB FAMILY: Operations Quality DIVISION: ANSC Nutrition Supply Chain LOCATION: Israel > Tel Aviv : Building 4 ADDITIONAL LOCATIONS: WORK SHIFT: Standard TRAVEL: Not specified MEDICAL SURVEILLANCE: Not Applicable SIGNIFICANT WORK ACTIVITIES: Not Applicable

About Aidoc Aidoc is the market leader in healthcare AI and has developed the world's largest clinical frontier model, supporting nearly 50 million patients each year. Aidoc is deployed in more than 2,000 medical centers worldwide. Since our founding in 2016, Aidoc has raised over $500 million and achieved a record number of FDA-cleared solutions. Medical diagnosis is hitting a breaking point, where the number of physicians hasn't kept up with the rapidly growing patient load. This leads to misdiagnosis and treatment delays that result in hundreds of thousands of deaths every year. Aidoc assists clinicians by precisely highlighting diseases directly on medical images, preventing misdiagnosis and ensuring that urgent patients receive the immediate attention they need. About the Role: We’re seeking a Senior Quality Specialist to join Aidoc’s QA team. In this role, you’ll lead the implementation and continuous improvement of quality assurance processes — including design controls, change control, and risk management, ensuring our products meet the highest global regulatory and industry standards. Your expertise will directly impact the safety, quality, and compliance of cutting-edge AI healthcare solutions. What You’ll Do: • Lead product release processes for new medical devices and software versions, collaborating closely with R&D, Product, Delivery, and SW QA teams. • Create, Maintain and review product related documentation (DHF, DMR, DHR, TFs) with a deep understanding of product design, implementation, and testing. • Translate regulatory requirements into actionable processes, enhancing efficiency, compliance, and product quality across the organization. • Support core QMS processes including SW Development Life Cycle (SDLC), Risk Management, CAPA, Non-Conformance, Usability, Document Control, Training, and more. • Leading AI and SW quality related problem solving • Cross-functional Collaboration: Work closely with SW engineers, data scientists, and product teams to identify testing requirements, troubleshoot issues, and improve overall AI system quality. • Assist in internal and external audits, ensuring readiness and full compliance. What You Bring: Education & Experience • Bachelor’s degree in Engineering, Life/Exact Sciences, Quality Assurance or Law. • 3+ years in the medical device industry, proven experience in QMS processes with a strong focus on SaMD (software as Medical Device). • Strong knowledge of FDA requirements, MDR regulation, ISO 13485, ISO 62304, ISO 14971 and IEC 62366. • Skilled in product risk assessment, requirements management and tracking, defect tracking, configuration management and how they are applied in the product development lifecycle • Experience improving processes, efficiency, and workflows. • Interest or background in computer science or AI — a plus. Skills & Qualities • Exceptional project and program management skills. • Structured thinker with the ability to drive cross-functional projects to completion. • Ability to work independently with minimal supervision • Detail-oriented, proactive, and accountable. • Strong communication skills in English, both written and verbal. • Collaborative, team-oriented mindset with a passion for learning and growth. Working at Aidoc - Our Perks: • Be part of something big - using cutting-edge technologies to transform the Healthcare industry (while saving patients’ lives) • We work in a hybrid model, with our new offices located at 34 HaMasger Street in Tel Aviv and parking for employees. • Amazing and healthy breakfasts and lunches prepared daily by our personal chef! • Stocked up kitchen & meal card • Wellness: Aidoc employees-only gym, plus Pilates, Yoga, and functional workouts classes. • Amazing culture - collaborative, transparent & fun! • Attractive compensation package & benefits Aidoc is deeply committed to creating an inclusive workplace, and to the principle of equal opportunity for all individuals. We prohibit discrimination and harassment based on race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or any other status protected by law.