Quality Assurance Specialist jobs in Israel

Job Description Summary Job Description Job Description 1. Site Preparation (Start-up): • Participate in site handover tasks and responsibilities and document them. • Develop mitigation plans for follow-up activities following the handover from the Project Quality Leader (PQL). • Participate in project site kick-off and review Quality Assurance (QA) contractual requirements. • Establish project-specific Supplier Quality Requirements (SQR) in coordination with the Supplier Quality organization. • Implement project-specific methods or procedures based on client requirements. • Take ownership of and apply the standard Inspection and Test Plan (ITP), updating it as necessary. • Review supplier documentation requests and update requirements according to contract specifics. • Analyze lessons learned from previous projects and propose applicable improvements. • Establish a project audit plan and conduct criticality assessments. • Create and obtain client approval for the Inspection and Test Plan for site assembly. • Prepare the site quality record book in accordance with contract and GE requirements. 2. Project Execution: • Collaborate with the Project Manager to ensure the implementation of quality plans and procedures. • Control document distribution, measuring devices, material traceability, and quality records. • Manage the registration and resolution of Non-Conformity Reports (NCR/NCM). • Produce inspection reports and maintain records of instruments and welder qualifications. • Supervise inspectors and inspection companies on-site. • Participate in audits and ensure that subcontractors have calibrated instruments. • Ensure all special processes are identified and personnel are properly qualified. • Collect and organize quality records for the site quality record book. • Conduct project audits and monitor corrective actions. • Manage non-conformities, root cause analysis, and corrective actions. • Provide QA performance statistics and manage client claims. 3. Project Closure (Pre-demobilization): • Drive the closure of open items such as punch lists and non-conformity issues. • Record lessons learned at the end of the project and ensure project files are closed. • Coordinate handover milestones and document "as-built" processes. Qualifications: • Bachelor’s degree in Mechanical Engineering or a related field. • Ability to work remotely at a hydroelectric power plant. • Extensive experience in quality engineering within construction or industrial projects. • Strong knowledge of quality management systems and standards. • Excellent analytical, problem-solving, and communication skills. • Ability to work collaboratively and manage multiple tasks effectively. • The candidate must possess an excellent level of English Desired Characteristics: • Professional Engineer (P.Eng) in mechanical engineering (preferred) from an accredited school. • 1 to 5 years of experience in heavy mechanical installation. • The candidate must have a strong personality and the ability to learn quickly. • The candidate must be bright and motivated by on-site heavy mechanical installation. • The candidate must have a good level of English. • The candidate will work at various power plant sites. Must be willing to travel and be present at the installation site full-time. Additional Information Relocation Assistance Provided: No #LI-Remote - This is a remote position

Description Bagira is a leader in the field of training and simulation systems with a track record of delivering high-end, customized, cost-effective solutions for mission readiness. Bagira’s simulators are being used by hundreds of thousands of soldiers at more than 80 sites worldwide. Bagira is looking for a QA Specialist to join our QA team at Bagira. The work is done in complex systems and involves close collaboration with the design, development and implementation teams. Ensure the quality Bagira’s software through the successful delivery in high quality of our products. This is a full-time position, based at our headquarters in Modi'in. What will your job look like: • Software testing • Design test cases and test plans • Defect reporting • Participation in factory acceptance tests (FAT) • Take active part in site acceptance tests (SAT) Requirements • Proven experience of at least 4 years in testing complex systems • Experience in planning and creating test documents and reporting bugs. • Motivate people without authority, strong collaboration skills • Experience in manual testing in an Agile environment - an advantage • Experience/ familiarity with military systems and/ or training - an advantage • Experience working on client side- an advantage • Ability to travel is required • Full proficiency in English Your Benefits In Bagira Communication, Ownership, Learnability, Impact, and Passion are the values that shape our culture and mindset. On top of openness, direct communication, independence, continuance learning, and lots of places to influence, we believe in the need to balance. As a Bagira employee, you will enjoy 4 annual quarterly days off, a day off to celebrate your birthday, a generous meal allowance, and many fun and happy moments.

Description Medison offers hope to patients suffering from rare and severe diseases by forming partnerships with emerging biotech companies to accelerate access to highly innovative therapies in international markets. As the creator and leader of the global partnership category in the pharma industry, we strive to be Always Ahead and work relentlessly to bring therapy to patients in need, no matter where they live. Our values are at the core of every action we take, and we are committed to going above and beyond to benefit the patients we serve. We are a dynamic, fast-paced company operating in over 34 countries on 5 continents. We are looking for out-of-the-box thinkers, people who are passionate, caring, agile, and adaptive, to join us on our mission. If you are looking to make a difference in people's lives, we invite you to join us! We are looking for a Quality Assurance Specialist to join our team. In this role you will be dealing with everything concerning quality & storage & distribution of drug products, according to GMP/GDP, from the minute it arrives at the Logistics Center until dispatched to customers. *This is a one-year temporary position. Responsibilities • Managing Quality Complaints • Supervising Packaging Adjustment • Conducting quality Control of incoming shipments • Conducting routing of Returned, Rejected, Recalled Products • Responsible for Packaging materials and relabeling • Handling Temperature Excursions, Deviations, Change Control and SOPs Requirements Required education and experience: • BA in Pharmacy + licensed by the Ministry of Health- Advantage, or BA in life sciences. • Experience as a licensed pharmacist with knowledge of Pharmacy laws- Advantage, or at least two years quality assurance experience in manufacturing or importation of pharmaceuticals. Required qualification: • High level of English and Hebrew. • Good knowledge of Microsoft Office - Outlook, PPT, Excel, and Word. • Detail-oriented with excellent multi-tasking abilities.

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

Description We are looking for a detail-oriented and proactive Quality Assurance Engineer to join our Quality team. In this role, you will be responsible for maintaining and continuously improving the organization's Quality Management System (QMS), ensuring compliance with industry standards, supporting audits, driving corrective actions, and contributing to operational excellence and product quality throughout the product realization lifecycle. • Lead NCR, MRB, 8D, and corrective action processes. • Administer quality software and maintain quality records. • Prepare monthly quality reports and KPI tracking. • Oversee Incoming Inspection of materials and parts • Follow up the Regulatory requirements for materials and prepare the relevant declarations • Handle the FAI reports’ preparation Please note: This position is focused on Quality Assurance within a manufacturing environment and is not related to Software QA or software testing roles. Requirements • B.Sc. in Engineering or related field. • Certified Quality Auditor/Engineer, advantage. • Minimum 3 years of experience in Quality Assurance / Quality Systems. • Experience with AS9100 environment, advantage. • Knowledge of Regulatory requirements for materials (RoHS, REACH, CMRT, California Proposition 65, etc.) • Fluent English and strong MS Office skills. • Detail-oriented and organized. • Ability to work independently and as part of a team. • Able to work effectively under pressure and meet deadlines.

אנחנו טבע אנחנו טבע, חברת ביו-פרמצבטית חדשנית ומובילה, המתבססת על מנוע גנרי ברמה עולמית. בין אם מדובר בחדשנות בתחומי מדעי המוח והאימונולוגיה או אספקת תרופות באיכות גבוהה, אנו מחויבים לתת מענה לצרכי המטופלים עכשיו ובעתיד. כאן, תהיו חלק מתרבות מכילה השואפת למצוינות, המעריכה חשיבה רעננה ושיתופי פעולה. יהיה לך מקום לצמוח, את הגמישות לאזן בין הבית לעבודה, ואת ההזדמנות להשפיע על בריאות טובה יותר ברחבי העולם, ביחד. הצוות שלנו וההשפעה שלך הזדמנות להיות הגורם שמתרגם תהליכי ייצור ואריזה סטריליים מורכבים לנהלים ברורים ומדויקים, ולהשפיע ישירות על איכות המוצר ועל העמידה בדרישות cGMP. איך יראה היום שלך ליישם את נהלי העבודה המחלקתיים ולעבוד בהתאם לדרישות ה-cGMP. לכתוב ולעדכן שיטות ייצור ואריזה ביחידה הסטרילית. לכתוב ולעדכן נהלי עבודה ומסמכים בהתאם לדרישות האתר. להכין חומרים להצגה ולהציגם בביקורת רגולטורית. לבצע תחקירים ולטפל בפעולות מתקנות ובקרות שינוי ביחידה הסטרילית. להוביל פרויקטי שיפור התיעוד במחלקות הייצור והאריזה. לשתף פעולה עם הבטחת האיכות וממשקים רבים לשיפור מדדי האיכות של האתר. לתעד ולעבוד מול מערכות ניהול איכות ובשיתוף הבטחת האיכות. הכישורים והניסיון שיש לך .תואר ראשון בהנדסה - הנדסת ביוטכנולוגיה, כימיה, מכונות, מדעי החיים .אנגלית ברמה גבוהה בכתב ובעל פה – לתקשורת מול הרשויות ובביקורות רגולטוריות .יכולות כתיבה גבוהות לצורך כתיבת חריגים, נהלים ושיטות עבודה. .עבודה מול ממשקים, הנעת תהליכים, ביצוע אסקלציות. .היכרות עם מערכות ניהול איכות – ייתרון גדול. .יתרון לניסיון בתעשיית הפארמה/מוצרים סטריליים. יתרון משמעותי .יכולת עבודה בצוות ובממשקים מרובים .תשומת לב לפרטים ותודעת איכות גבוהה .יכולת עמידה בלוחות זמנים ותיעדוף משימות .אסרטיביות ויכולת הנעת תהליכים .למידה עצמית והסתגלות מהירה לשינויים How We’ll Take Care of You At Teva, better health starts from within, and that includes you. From day one, you’ll be supported with benefits designed to help you thrive in and out of work. This includes generous annual leave, reward plans, flexible working schedules (dependent on role), access to tailored health support, and meaningful ways to give back to the community.  When it comes to your career, you’ll be encouraged to explore, evolve, and shape your path. Twist, our one-stop shop for career development platform, gives you access to a wide range of possibilities, from learning programs and short-term projects to opportunities for internal growth. Here, you’ll be part of a culture that empowers you to reach your goals and prioritize your wellbeing every step of the way.  Already Working @Teva? Make sure to apply through our internal career site on Twist—your one-stop shop for career development Teva’s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.

Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact. A Day in the Life As a Senior Manufacturing Quality Engineer , you will play a key role in ensuring that products are manufactured in compliance with internal quality standards, regulatory requirements, and Medtronic’s commitment to patient safety and product excellence. This position partners closely with Manufacturing, Operations, R&D, and Supply Chain to drive quality improvements and support continuous improvement initiatives on the production floor. This is a temporary, 1-year contract role responsible for ensuring compliance, quality, and operational excellence throughout the development and manufacturing of Class III medical devices. Primary Responsibilities: • Maintain and continuously improve the Quality Management System in compliance with ISO 13485, EU MDR, and FDA QSR (21 CFR 820) • Support Operations activities, including manufacturing, validation, MRB, CAPA. • Oversee CAPA, nonconformances, deviations, complaints, risk management, change controls, document control, and training processes. • Actively participate in and support internal and regulatory audits, including preparation, execution, and follow-up. • Collaborate cross-functionally with R&D, Regulatory Affairs, Operations, and Supply Quality teams. • Support production, engineering, validation activities including training, reviewing and approving documentation, work instructions, SOPs , supporting risk assessments, to ensure compliance with regulatory and quality system requirements. • Lead and support investigations of nonconformances, deviations, and CAPAs, including root cause analysis and implementation of corrective and preventive actions. Required Qualifications: • Bachelor’s degree in Engineering, Biotechnology, Life Sciences, or a related field. • 4+ years of QA production experience within the medical device industry. • In-depth knowledge of FDA 21 CFR Part 820, ISO 13485/14971, and EU MDR. • Hands-on experience with ECO’s, nonconformance management, CAPA, and root cause analysis tools. • Strong communication skills in English, both written and verbal. Preferred Qualifications: • Knowledge of Lean, Six Sigma, or continuous improvement methodologies. • Ability to work effectively in a cross-functional, fast-paced manufacturing environment. Physical Job Requirements The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.  ‌ ‌ Recruitment Fraud Alert We are aware of phishing scams targeting job seekers. Please keep the following in mind: Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.com email addresses. Medtronic will never ask for payment or sensitive personal information (such as bank account or Social Security details) during early stages of the hiring process. Any such requests are not legitimate. If you receive a suspicious message claiming to be from Medtronic, do not respond, click links, or open attachments. If you have any questions, concerns regarding the authenticity of a communication alleged to have been made by or on behalf of Medtronic, please contact us immediately at [email protected]. Benefits & Compensation Medtronic offers a competitive Salary and flexible Benefits Package A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. ‌ This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).

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.