About AbbVie AbbVie’s mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women’s health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. We are recruiting a Senior Manager for the Quality Assurance Department at the Lod site. As part of thr job: 1. Assure quality process and procedures are effective and in compliance with the regulations. Support internal/external Regulatory inspections. 2. Prepare, review and approve Quality system records. Makes decisions that may affect product disposition or have adverse consequences on the Quality system. 3. Lead a group of professional responsible of the quality activities execution. Provide guidance and quality expertise. 4. Lead Quality Plan and Improvement projects. Responsible for planning, implementation, tracking and reporting of the Quality plan projects and strategic initiatives at the site. 5. Perform assessments to determine compliance to processes and regulation. Identify gaps a mitigate and implement improvements 6. Coordinate and support Quality Reviews with executive management. Assure that the actions are assigned ,tracked and completed . 7. Provide direction to ensure sources of product and quality problems are identified. Provide leadership to ensure that CAPA actions are adequate and implemented in a timely manner. 8. Provide consultation and training on Quality expertise to internal and cross functional groups. 9.Review Technical information provided to support the Quality system. Assure that the correct techniques and tools are used. 10. Advocate for continual improvement of operations and Quality system. Qualifications Bachelor's degree in Science(Chemistry, Pharmacy, Biology , Microbiology , Engineering or other technical/scientific area) . Master degree is desirable. 8 years minimum experience in quality assurance, technical field on a regulated industry or relevant experience. Technical knowledge in as many of the following areas as possible: Quality, Regulatory, process technology, manufacturing operations, project management Fluent Hebrew and English - must! Come and join our taem! Travel No Job Type Experienced Schedule Full-time Job Level Code IC Equal Employment Opportunity At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic.