Quality Control Manager jobs in Israel

Description The Senior Quality Assurance Manager is responsible for leading all quality, compliance, reliability, testing, and qualification activities across the Foil Division. The role ensures compliance with customer, regulatory, military, and corporate requirements while driving operational excellence, continuous improvement, and customer satisfaction. As a key business partner to Operations, Engineering, R&D, Supply Chain, and Commercial teams, this leader will oversee the Quality Management System, Calibration Laboratory activities, Reliability & Testing Laboratory operations, product qualification activities, and audit readiness across the organization. Please note: This position is focused on Quality Assurance within a manufacturing environment and is not related to Software QA or software testing roles. Key Responsibilities Quality Leadership & Compliance • Lead and manage all Quality Assurance and Quality Control activities across the Foil Division in accordance with local QMS and corporate quality procedures. • Maintain and continuously improve the Quality Management System (QMS) in VFR in accordance with AS9100, MIL-STD-790 and CECC. • Serve as the focal point for certifications, regulatory compliance, customer audits, and quality system assessments. • Ensure ongoing readiness for customers, certification, regulatory, and military audits. • Develop quality strategy, KPIs, and continuous improvement initiatives. Reliability Laboratory & Product Qualification • Lead the Reliability & Testing Laboratory, ensuring resources, capabilities, equipment readiness, and testing performance support business and customer needs. • Lead Maintenance Activities of existing product qualifications (QPL, CECC). • Oversee product qualification, validation, reliability testing, and compliance with customer and industry specifications (MIL-PRF, NASA & ESA, automotive, etc.) • Manage laboratory priorities, personnel, and continuous improvement programs. • Support internal development programs and external customer testing activities. Metrology & Calibration Management • Own the site calibration and metrology systems, ensuring compliance and traceability of measurement and test equipment. • Oversee calibration programs, measurement system effectiveness, and related compliance requirements. Customer & Supplier Quality • Lead customer quality improvement initiatives, complaint resolution (FA , root cause investigations, and corrective actions). • Oversee supplier qualification, supplier performance, audits, and change management processes. • Act as the primary quality representative to customers and external stakeholders. Operational & Organizational Leadership • Drive process improvements that enhance product quality, reliability, efficiency, and customer satisfaction. • Lead, develop, and mentor quality managers, engineers, technicians, and inspectors. • Manage departmental priorities, budgets, resources, and strategic plans. • Collaborate closely with Operations, Engineering, R&D, Supply Chain, and Commercial teams to support business growth and operational excellence. Requirements Education • B.Sc. or M.Sc. in Engineering, Materials Science, Physics, Electronics, Quality Engineering, or a related field. • Quality certifications such as CQE, CQM, Lead Auditor, or equivalent are an advantage. Experience • 8+ years of proven quality leadership experience in a highly regulated manufacturing environment. • Background in aerospace, defense, electronics, precision manufacturing, automotive, medical equipment industries is preferred. • Experience with reliability testing, testing laboratory operations, qualification programs, and metrology systems is an advantage.

We Are Teva We’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we’re dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together. Our Team, Your Impact The Director, Site Quality Control is responsible for leading and managing all QC laboratory operations at the Kfar Saba site, ensuring testing, release, and analytical activities comply with global regulations, compendial standards, and Teva Quality policies. This role leads a key QC function at one of Teva’s flagship production sites, ensuring compliant supply of high‑quality medicines while shaping global quality outcomes. How You’ll Spend Your Day • Lead all QC laboratory units including Raw Materials QC, Finished Goods QC, , Stability, Analytical Development support and laboratories logistics • Develop QC strategy aligned with site priorities, supply needs, and compliance expectations. • Oversee QC deviations, OOS/OOT investigations, and laboratory CAPAs, ensuring timely closure and robust root cause analysis. • Ensure timely release of RM and FG, manage analytical bottlenecks, backlog reduction, and lab capacity planning. • Ensure audit/inspection readiness and represent QC during regulatory inspections. • Drive QC process optimization, automation, and efficiency improvements. • Partner with QA, MS&T, Engineering, Supply Chain, and R&D on investigations, analytics, and tech transfers. • Lead QC support for new product launches, validation batches, and market supply escalations. • Lead TLMS deployments in all laboratories Your Skills and Experience • Bachelor’s or Master’s degree in Chemistry, Life Sciences, Pharmacy, or related scientific discipline. • 12+ years of progressive QC experience in the pharmaceutical industry. • Significant leadership experience managing QC laboratories in a regulated GMP environment. • Strong understanding of analytical chemistry, microbiology, methods, and compendial standards. • Experience interacting with health authorities (FDA, EMA, EDQM). Also Good to Have • Strong leadership, communication, and stakeholder‑management skills. • Data‑driven decision‑making with focus on performance and reliability. • Excellent problem‑solving and root‑cause analysis abilities. • High resilience and ownership mindset. • Ability to manage multiple priorities in a dynamic, regulated environment. 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.  Reports To Sr Director, Site Quality Head – Kfar Saba 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.